Tag: M.W=150-200

Cavallaro, G. published the artcileNovel Cationic Copolymers of a Polyasparthylhydrazide: Synthesis and Characterization, HPLC of Formula: 6249-56-5, the publication is Drug Delivery (2005), 12(6), 377-384, database is CAplus and MEDLINE.

α,β-Poly(asparthylhydrazide) (PAHy), a water soluble synthetic polymer, was functionalized by using EDCI chem. with 3-(carboxypropyl)trimethyl-ammonium chloride (CPTACl) obtaining carboxypropyltrimethyl ammonium copolymers (PAHy-CPTA). Three PAHy-CPTA copolymers at increasing derivatization degrees (38%, 48%, 58%) were chosen for subsequent investigations. The capability of these copolymers to bind, neutralize, and protect DNA against degradation by DNase II was evaluated by gel retardation assay and DNA degradation test at pH 5.5. Zeta potential measurements show that all studied polymers are able to neutralize the anionic charge of DNA at polymer/DNA weight ratio in the range of 0.8/1-5/1. Polyplex dimensional distribution analyses in distilled water, saline solution NaCl 0.9%, and HEPES pH 7 show that polyplex size is strongly affected by both presence and type of electrolyte and with time incubation.

Drug Delivery published new progress about 6249-56-5. 6249-56-5 belongs to chlorides-buliding-blocks, auxiliary class Phase Transfer Catalyst,Inhibitor,Natural product, name is 3-Carboxy-N,N,N-trimethylpropan-1-aminium chloride, and the molecular formula is C7H16ClNO2, HPLC of Formula: 6249-56-5.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Huang, Zhaoxiang published the artcileSynergistic effects of cinnamaldehyde and cinnamic acid in cinnamon essential oil against S. pullorum, Category: chlorides-buliding-blocks, the publication is Industrial Crops and Products (2021), 113296, database is CAplus.

Cinnamon is an important spice crop that is widely cultivated in tropical regions. In this study, the antibacterial activities of four accessions of cinnamon essential oil (CEO) belonging to three different species (CEO1 and CEO4, Cinnamomum cassia Presl. (Lauraceae) bark; CEO2, Cinnamomum zeylanicum Blume (Lauraceae) bark; CEO3, Cinnamomum burmannii Blume (Lauraceae) bark) toward Salmonella enterica subsp. enterica serovar pullorum (S. pullorum) were evaluated by microdilution assay and kinetic anal. The min. inhibitory concentration (MIC) of the CEOs were all 0.31 mg/mL, and kinetic anal. suggested that the lag phase and maximum specific growth rate of bacteria were concentration dependent. Furthermore, to explore the synergistic antibacterial effects between main components and minor components, the volatile constituents of CEOs were determined by gas chromatog.-mass spectrometry (GC-MS). Cinnamaldehyde (CM) (57.73 %-91.79 %) was the principal constituent in CEO1-CEO4 (p < 0.05), with CEO3 having the highest CM contents. A synergistic effect against S. pullorum was observed when CA was combined with CM. To explore the potential synergistic mechanism, the membrane glycerophospholipid (GPL) composition of S. pullorum was characterized by ultra-performance liquid chromatog.-tandem mass spectrometry (UPLC-MS/MS). CM, CA, and their combination regulated the levels of most phosphatidylethanolamines (PEs), phosphatidylglycerols (PGs), phosphatidic acids (PAs), and some cardiolipins (CLs).

Industrial Crops and Products published new progress about 620-20-2. 620-20-2 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Benzyl chloride,Benzene, name is 3-Chlorobenzylchloride, and the molecular formula is C7H6Cl2, Category: chlorides-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Tsoung, Jennifer published the artcileMulticomponent-Multicatalyst Reactions (MC)²R: Efficient Dibenzazepine Synthesis, Quality Control of 145349-62-8, the publication is Organic Letters (2014), 16(1), 110-113, database is CAplus and MEDLINE.

A Rh^I/Pd⁰ catalyst system was applied to the multicomponent synthesis of azadibenzazepines from vinylpyridines, arylboronic acids, and amines in a domino process with no intermediate isolation or purification E.g., a combination of 3-chloro-5-(trifluoromethyl)-2-vinylpyridine, 2-chlorophenylboronic acid, and p-toluidine was added to a catalyst solution containing Pd precatalyst (I, L = RuPhos), XPhos, and [Rh(cod)OH]₂ to give a 67% yield of 5-(p-tolyl)-3-(trifluoromethyl)-10,11-dihydro-5H-benzo[b]pyrido[2,3-f]azepine (II).

Organic Letters published new progress about 145349-62-8. 145349-62-8 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Boronic acid and ester,Benzene,Boronic Acids, name is 2-Chloro-4-methylphenylboronic acid, and the molecular formula is C5H6BNO2, Quality Control of 145349-62-8.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Licciardi, Mariano published the artcileCationic Supramolecular Vesicular Aggregates for Pulmonary Tissue Selective Delivery in Anticancer Therapy, Application of 3-Carboxy-N,N,N-trimethylpropan-1-aminium chloride, the publication is ChemMedChem (2016), 11(16), 1734-1744, database is CAplus and MEDLINE.

The biopharmaceutical properties of supramol. vesicular aggregates (SVAs) were characterized with regard to their physicochem. features and compared with cationic liposomes (CLs). Neutral and cationic SVAs were synthesized using two different copolymers of poly(aspartyl hydrazide) by thin-layer evaporation and extrusion techniques. Both copolymers were self-assembled in pre-formulated liposomes and formed neutral and cationic SVAs. Gemcitabine hydrochloride (GEM) was used as an anticancer drug and loaded by a pH gradient remote loading procedure, which significantly increased drug loading inside the SVAs. The resulting average size of the SVAs was 100 nm. The anticancer activity of GEM-loaded neutral and cationic SVAs was tested in human alveolar basal epithelial (A549) and colorectal cancer (CaCo-2) cells. GEM-loaded cationic SVAs increased the anticancer activity in A549 and CaCo-2 cells relative to free drug, neutral SVAs, and CLs. In vivo biodistribution in Wistar rats showed that cationic SVAs accumulate at higher concentrations in lung tissue than neutral SVAs and CLs. Cationic SVAs may therefore serve as an innovative future therapy for pulmonary carcinoma.

ChemMedChem published new progress about 6249-56-5. 6249-56-5 belongs to chlorides-buliding-blocks, auxiliary class Phase Transfer Catalyst,Inhibitor,Natural product, name is 3-Carboxy-N,N,N-trimethylpropan-1-aminium chloride, and the molecular formula is C7H16ClNO2, Application of 3-Carboxy-N,N,N-trimethylpropan-1-aminium chloride.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Guiheneuf, Solene published the artcileMicrowave Assisted Organic Synthesis (MAOS) of New Dispacamide A Derivatives Bearing a Thiazolinone Platform, Biological Assays on Inhibition of Protein Kinases and Cell Effects, Computed Properties of 3696-23-9, the publication is Current Microwave Chemistry (2014), 1(1), 33-40, database is CAplus.

A series of (5Z)-5-ylidene-thiazolidine-4-one derivatives bearing the N-(4,5-dihalogenopyrrol-2-yl)carbamoyl fragment of Dispacamide A was prepared through a newly developed approach using a solution phase protocol assisted by microwave irradiation These new compounds were synthesized in good yields (10-98%) by sulfur/nitrogen displacement or eventually by Knoevenagel condensation in the presence of a base (AcONa) in AcOH solution The ten synthetic products have been obtained with a Z-geometry about their exocyclic double bond. All these compounds have been evaluated against eight protein kinases and human cell lines.

Current Microwave Chemistry published new progress about 3696-23-9. 3696-23-9 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Thiourea,Amine,Benzene,Amide, name is 1-(4-Chlorophenyl)thiourea, and the molecular formula is C7H7ClN2S, Computed Properties of 3696-23-9.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Rhee, Hee-Kyung published the artcileSynthesis, cytotoxicity, and DNA topoisomerase II inhibitory activity of benzofuroquinolinediones, Application In Synthesis of 4584-49-0, the publication is Bioorganic & Medicinal Chemistry (2007), 15(4), 1651-1658, database is CAplus and MEDLINE.

Benzofuroquinolinediones (7c and 7d) were synthesized by base-catalyzed condensation of dichloroquinolinediones with phenolic derivatives Their dialkylaminoalkoxy derivatives (8i-8p) were prepared by reaction with various dialkylaminoalkyl chlorides. The cytotoxicity of the synthesized compounds was evaluated against eight types of human cancer cell lines, and their topoisomerase II inhibition was assessed. In general, the cytotoxicity of benzofuroquinolinediones (8i-8p) was similar or superior to that of doxorubicin and showed more potent inhibitory activity than naphthofurandiones (8a-8h). Also, most of the compounds exhibited excellent topoisomerase II inhibitory activity at a concentration of 5 μM and two compounds, 8d and 8i, showed IC₅₀ values of 1.19 and 0.68 μM, resp., and were much more potent than etoposide (IC₅₀ = 78.4 μM), but similar to doxorubicin (IC₅₀ = 2.67 μM). However their inhibitory activity on topoisomerase I was lower, and 8d and 8i showed IC₅₀ values of 42.0 and 64.3 μM, resp.

Bioorganic & Medicinal Chemistry published new progress about 4584-49-0. 4584-49-0 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Salt,Amine,Aliphatic hydrocarbon chain, name is 2-Chloro-N,N-dimethylpropan-1-amine hydrochloride, and the molecular formula is C5H13Cl2N, Application In Synthesis of 4584-49-0.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Walton, E. published the artcileNew analgesics. III. Homologs of amidone, isoamidone, and some related compounds, Product Details of C5H13Cl2N, the publication is Journal of the Chemical Society (1949), 648-55, database is CAplus.

cf. C.A. 42, 6814d. In view of the established value of amidone (Me₂NCHMeCH₂CPh₂COEt) as an analgesic, 4 series of related ketones have been prepared by condensing Ph₂CHCN with a Cl base and treating the resulting basic cyanides with Grignard reagents. In general, the analgesic and respiratory depression activities remain associated but not always in the same ratio, maximum activity being attained in the Et ketone in all 4 series. Data are given for the analgesic activity, respiratory depression activity, approx. LD₅₀ (i.v. injection into mice), and toxic concentration on isolated rabbit heart. MeCH(NMe₂)CH₂OH (32 g.) and 46 mL. SOCl₂ in 120 mL. CHCl₃, warmed 3 h., give 1-chloro-2-(dimethylamino)propane-HCl, deliquescent, m. 101-2°; heated 3 min. at 140-60°, it yields MeCHClCH₂NMe₂.HCl (not changed by heating at 190-200°), which results also from MeCH(OH)CH₂NMe₂ and SOCl₂. A mixture of 26 g. Me₂NCHMeCH₂CPh₂CN (I) and Me₂NCH₂CHMeCPh₂CN (II) (prepared by the German process, Rept. Number P.B. 981, Office of the Pub. Board, Wash., D. C., p. 84) crystallized from petr. ether (b. 60-80°), gives 13.5 g. I, m. 90-1° (HCl salt, m. 181-3°; HBr salt, m. 175°; HI salt, cream, m. 203-4°; nitrate, m. 168-70° (decomposition); methiodide, m. 238-46°); the oil from the mother liquor of I, treated with 40% HBr, gives 14 g. of the HBr salt, m. 223-4°, of II, m. 68-9°; HCl salt, m. 224-5°; HI salt, m. 212-13°; nitrate, m. 178° (decomposition); H D-tartrate, m. 88-98°; methiodide, m. 235-45°. I (5 g.) in 20 mL. xylene and MeMgI (7.7 g. MeI), heated 2 h. on the steam bath (ether allowed to evaporate) and 2 h. on a sand bath, give 5-dimethylamino-3,3-diphenyl-2-hexanone, m. 72-3° (HCl salt, m. 185-7°; HBr salt, m. 193-5°; HI salt, m. 180-2°). Amidone (III) (m. 80-2°) yields a HI salt, m. 198-9°, a nitrate m. 108-10° (decomposition), and a methiodide, m. 168-70°. I and PrMgI give 7-dimethylamino-5,5-diphenyl-4-octanone which yields a nitrate, m. 95-7°, a HI salt, m. 155-7°, and a HBr salt, m. 87-9°. I and iso-PrMgBr give 6-dimethylamino-4,4-diphenyl-2-methyl-3-heptanone, b₄ 176-86° (nitrate, m. 116-18°). I and BuMgI yield 2-dimethylamino-4,4-diphenyl-5-nonanone, characterized as the HCl salt, m. 83-6°; HBr salt, m. 103-5°; HI salt, m. 140-3°, and nitrate, m. 77-8°. I and PhMgBr give the intermediate ketimine (C₂₅H₂₈N₂.HCl), m. 136-8°; refluxed 2 h. with 20% HBr, this yields the HBr salt, m. 181-3°, of Ph 3-dimethylamino-1,1-diphenylbutyl ketone; HCl salt, m. 197-8°. I and PhCH₂MgBr give 5-dimethylamino-1,3,3-triphenyl-2-hexanone-HCl, m. 236-7°; HBr salt, m. 243-4°. I (40 g.) and 21.6 g. D-tartaric acid in 430 mL. Me₂CO and 10 mL. H₂O, kept 24 h. at 0°, give 28 g. of the H D-tartrate, m. 109-12°, [α]_D²⁰ 16° (H₂O), of (-)-I, m. 99-101°, [α]_D²¹ -51° (EtOH); the Me₂CO mother liquors plus a little ether, kept 4 days at 0°, give 14 g. of the H D-tartrate, m. 66-70°, [α]_D²⁰ 5° (H₂O), of (+)-I, m. 101°, [α]_D²² 49° (EtOH); HBr salt, m. 216-18°, [α]_D²² 5 (EtOH), -4° (H₂O); nitrate, m. 169-71° (decomposition), [α]_D²⁰ 5° (EtOH), -6° (H₂O). (-)-I and EtMgBr give (-)-III, m. 99-101°, [α]_D²² -32° (EtOH); HBr salt, m. 234-5°, [α]_D²² -134° (EtOH); HCl salt, m. 241-2° (decomposition), [α]_D²¹ -130° (H₂O). (+)-III, m. 98-100°, [α]_D²⁰ 28° (EtOH); HI salt, m. 175-7° (decomposition); nitrate, m. 148° (decomposition), [α]_D¹⁹ 137° (EtOH). I (2 g.), 4 mL. concentrated H₂SO₄, and 4 mL. H₂O, refluxed 20 min., give 2.3 g. of the acid sulfate, m. 222-3°, of γ-dimethylamino-α,α-diphenylvaleric acid (IV), m. 198-9° (decomposition); HCl salt, m. 213-16°; the mother liquor yields the amide, m. 175-6° (HCl salt, m. 190-1°); Me ester, m. 60-5° [HCl salt, m. 166-8° (decomposition); HBr salt, m. 182° (decomposition)]; Et ester, an oil (HBr salt, m. 167-8°). I (5 g.), 0.7 g. NaNH₂, and 10 mL. PhMe, refluxed 6-7 h., give 2.5 g. I and 3-dimethylamino-1,1-diphenylbutane, whose HBr salt m. 159-60°; it results also on heating IV 15 min. at 200°; methiodide, m. 195-6°. IV (0.8 g.) and 0.5 mL. SOCl₂ in CHCl₃, warmed 4 h. on the steam bath, give 3,3-diphenyl-1,5-dimethyl-2-pyrrolidone, m. 122-3°. II and MeMgI in xylene, heated 1 h. on the steam bath and refluxed 1 h., give the ketimine (methiodide, C₂₁H₂₉N₂I, decompose 176-230°), which yields 5-dimethylamino-3,3-diphenyl-4-methyl-2-pentanone, m. 61-5° (HBr salt, m. 194-6°). II (16.6 g.) and EtMgBr give the ketimine, b₁ 94° (methiodide, m. 240°); refluxed 2.5 h. with 20% HBr, it yields 10.3 g. 6-dimethylamino-4,4-diphenyl-5-methyl-3-hexanone-HBr, m. 139-44°; HI salt, m. 206-8°; nitrate, m. 182-3° (decomposition); H D-tartrate, m. 150-4°. II (16.6 g.) and PrMgBr give 3.75 g. of the HCl salt, m. 80-100°, of 1-dimethylamino-3,3-diphenyl-2-methyl-4-heptanone, m. 100-1°. II and 5 mols. iso-PrMgBr give 6-dimethylamino-4,4-diphenyl-2,5-dimethyl-3-hexanone, whose HBr salt m. 81-5°. II and excess 48% HBr, heated 3.5 h. at 180°, give 3,3-diphenyl-1,4-dimethyl-2-pyrrolidone, m. 121-3°. Ph₂CHCN (67.2 g.), 22 g. Me₂N(CH₂)₂CN, and 6.8 g. NaNH₂ in 200 mL. C₆H₆ give 39 g. crude 3-dimethylamino-1,1-diphenylpropyl cyanide (V); HCl salt, m. 196-7°; HI salt, m. 221-3°. V (14 g.) gives 9 g. 5-dimethylamino-3,3-diphenyl-2-pentanone (HCl salt, m. 152-3°); EtMgBr gives 6-dimethylamino-4,4-diphenyl-3-hexanone (HCl salt, m. 171-2°); PrMgI gives 1-dimethylamino-3,3-diphenyl-4-heptanone (HI salt, m. 156-7°); iso-PrMgBr yields 6-dimethylamino-4,4-diphenyl-2-methyl-3-hexanone (HBr salt, m. 104-6°). 3-(1-Piperidyl)-1,1-diphenylpropyl cyanide (VI), m. 73-4° [HCl salt, m. 196-7°; HBr salt, m. 185-6°; HI salt, m. 152-3°; nitrate, m. 155° (decomposition)]. VI and MeMgI give 5-(1-piperidyl)-3,3-diphenyl-2-pentanone (HBr salt, m. 162-3°; HI salt, m. 158-9°); EtMgI yields 6-(1-piperidyl)-4,4-diphenyl-3-hexanone (HBr salt, m. 192-3°); PrMgI gives 1-(1-piperidyl)-3,3-diphenyl-4-heptanone (HCl salt, m. 158-60°; HI salt, m. 217-20°). VI and PhMgBr give Ph 3-(1-piperidyl)-1,1-diphenylpropyl ketone-HBr, m. 191-3°. VI (1.9 g.) and 3.6 mL. H₂SO₄, refluxed 30 min., give 0.5 g. α,α-diphenyl-1-piperidinebutyric acid, m. 230-5° (decomposition) (HCl salt, m. 236° (decomposition); H sulfate, m. 105-14°), and 0.6 g. of the amide, m. 178-9°; Me ester-HBr, with 2 mols. H₂O, m. 78-82°; Et ester-HBr, m. 194-6°. VI (2.3 g.), 0.9 g. NaNH₂, and 25 mL. C₆H₆, refluxed 3 h., give 3-(1-piperidyl)-1,1-diphenylpropane-HCl, m. 208-10°.

Journal of the Chemical Society published new progress about 4584-49-0. 4584-49-0 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Salt,Amine,Aliphatic hydrocarbon chain, name is 2-Chloro-N,N-dimethylpropan-1-amine hydrochloride, and the molecular formula is C4H6O3, Product Details of C5H13Cl2N.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Wakatake, Takanori published the artcileAn auxin transport network underlies xylem bridge formation between the hemi-parasitic plant Phtheirospermum japonicum and host Arabidopsis, Product Details of C8H7ClO3, the publication is Development (Cambridge, United Kingdom) (2020), 147(14), dev187781, database is CAplus and MEDLINE.

Parasitic plants form vascular connections with host plants for efficient material transport. The haustorium is the responsible organ for host invasion and subsequent vascular connection. After invasion of host tissues, vascular meristem-like cells emerge in the central region of the haustorium, differentiate into tracheary elements and establish a connection, known as a xylem bridge, between parasite and host xylem systems. Despite the importance of this parasitic connection, the regulatory mechanisms of xylem bridge formation are unknown. Here, we show the role of auxin and auxin transporters during the process of xylem bridge formation using an Orobanchaceae hemiparasitic plant, Phtheirospermum japonicum. The auxin response marker DR5 has a similar expression pattern to tracheary element differentiation genes in haustoria. Auxin transport inhibitors alter tracheary element differentiation in haustoria, but biosynthesis inhibitors do not, demonstrating the importance of auxin transport during xylem bridge formation. The expression patterns and subcellular localization of PIN family auxin efflux carriers and AUX1/LAX influx carriers correlate with DR5 expression patterns. The cooperative action of auxin transporters is therefore responsible for controlling xylem vessel connections between parasite and host.

Development (Cambridge, United Kingdom) published new progress about 33697-81-3. 33697-81-3 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Carboxylic acid,Benzene,Phenol, name is 3-Chloro-4-hydroxyphenylacetic acid, and the molecular formula is C6H4ClNO2, Product Details of C8H7ClO3.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Komatsu, Ryutaro published the artcileManipulating the Electronic Excited State Energies of Pyrimidine-Based Thermally Activated Delayed Fluorescence Emitters To Realize Efficient Deep-Blue Emission, Recommanded Product: 4-Chloro-2-methylphenylboronic acid, the publication is ACS Applied Materials & Interfaces (2017), 9(5), 4742-4749, database is CAplus and MEDLINE.

The electronic excited state energies of pyrimidine-based TADF emitters were molecularly manipulated to realize deep-blue emission and reduced delayed fluorescent lifetime (τ_d). The authors then systematically studied the relations among the chem. structure, properties, and device performances. The resultant novel pyrimidine emitters, called Ac-XMHPMs (X = 1, 2, and 3), contain different numbers of bulky Me substituents at acceptor moieties, increasing the excited singlet (E_S) and triplet state (E_T) energies. Among them, Ac-3MHPM, with a high E_T of 2.95 eV, exhibited a high external quantum efficiency (η_ext,max) of 18% and an η_ext of 10% at 100 cd m^-2 with Commission Internationale de l’Eclairage chromaticity coordinates of (0.16, 0.15). These efficiencies are among the highest values to date for deep-blue TADF OLEDs. The mol. design strategy provides fundamental guidance to design novel deep-blue TADF emitters.

ACS Applied Materials & Interfaces published new progress about 209919-30-2. 209919-30-2 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Boronic acid and ester,Benzene,Boronic Acids,Boronic acid and ester, name is 4-Chloro-2-methylphenylboronic acid, and the molecular formula is C7H8BClO2, Recommanded Product: 4-Chloro-2-methylphenylboronic acid.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Sano, Mitsuji published the artcileField desorption mass spectrometry of betaine hydrohalides, Recommanded Product: 3-Carboxy-N,N,N-trimethylpropan-1-aminium chloride, the publication is Biomedical Mass Spectrometry (1982), 9(10), 438-42, database is CAplus.

The field desorption mass spectra of betaine hydrohalides (e.g. Me₃N⁺CH₂CO₂H Cl^–) and I were examined Field desorption ions, [betaines +H]⁺, and cluster ions, [nbetaines +H]⁺, were generally observed In compounds where the conformation between the quaternary ammonium N atom and the CO₂H group prohibits betaine formation, the spectra consist only of complex field desorption ions due to thermal decomposition products. Quaternary ammonium cations and cluster ions which arise from ordinary quaternary ammonium compounds are hardly produced. The effect of counter ions and the mechanism of field desorption ion formation are discussed.

Biomedical Mass Spectrometry published new progress about 6249-56-5. 6249-56-5 belongs to chlorides-buliding-blocks, auxiliary class Phase Transfer Catalyst,Inhibitor,Natural product, name is 3-Carboxy-N,N,N-trimethylpropan-1-aminium chloride, and the molecular formula is C7H16ClNO2, Recommanded Product: 3-Carboxy-N,N,N-trimethylpropan-1-aminium chloride.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics