Tag: 100-200

Synthesis, structural elucidation, and antibacterial evaluation of some flavones derived from coumarin was written by Chavhan, JV.;Patil, SS.. And the article was included in International Journal of Pharmaceutical, Chemical and Biological Sciences in 2018.Recommanded Product: 4-Chlororesorcinol The following contents are mentioned in the article:

In the present study, substituted coumarin-based flavones I (R = OH, Cl) were synthesized via chalcones. The reactions were easily conducted under mild conditions and gave I in good yields. The synthesized compounds were evaluated against four strains of bacterial culture. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Recommanded Product: 4-Chlororesorcinol).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Recommanded Product: 4-Chlororesorcinol

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Ni-Catalyzed Carboxylation of Unactivated Alkyl Chlorides with CO₂ was written by Borjesson, Marino;Moragas, Toni;Martin, Ruben. And the article was included in Journal of the American Chemical Society in 2016.Computed Properties of C6H12BrCl The following contents are mentioned in the article:

A catalytic carboxylation of unactivated primary, secondary, and tertiary alkyl chlorides with CO₂ at atm. pressure is described. This protocol represents the first intermol. cross-electrophile coupling of unactivated alkyl chlorides, thus leading to new knowledge in the cross-coupling arena. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Computed Properties of C6H12BrCl).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Computed Properties of C6H12BrCl

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Dual Catalytic Platform for Enabling sp³ α C-H Arylation and Alkylation of Benzamides was written by Rand, Alexander W.;Yin, Hongfei;Xu, Liang;Giacoboni, Jessica;Martin-Montero, Raul;Romano, Ciro;Montgomery, John;Martin, Ruben. And the article was included in ACS Catalysis in 2020.Safety of 1-Bromo-6-chlorohexane The following contents are mentioned in the article:

A dual catalytic sp³ α C-H arylation and alkylation of benzamides with organic halides is described. This protocol exhibits an exquisite site selectivity, chemoselectivity, and enantioselectivity pattern, offering a complementary reactivity mode to existing sp³ arylation or alkylations via transition metal catalysis or photoredox events. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Safety of 1-Bromo-6-chlorohexane).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Safety of 1-Bromo-6-chlorohexane

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

C-C Bond Formation via Copper-Catalyzed Conjugate Addition Reactions to Enones in Water at Room Temperature was written by Lipshutz, Bruce H.;Huang, Shenlin;Leong, Wendy Wen Yi;Isley, Nicholas A.. And the article was included in Journal of the American Chemical Society in 2012.Category: chlorides-buliding-blocks The following contents are mentioned in the article:

Conjugate addition reactions to enones can now be done in water at room temperature with in situ generated organocopper reagents. Mixing an enone, zinc powder, TMEDA, and an alkyl halide in a micellar environment containing catalytic amounts of Cu(I), Ag(I), and Au(III) leads to 1,4-adducts in good isolated yields: no organometallic precursor need be formed. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Category: chlorides-buliding-blocks).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Category: chlorides-buliding-blocks

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Palladium-Catalyzed Hydroalkylation of Styrenes with Organozinc Reagents To Form Carbon-Carbon sp³-sp³ Bonds under Oxidative Conditions was written by Urkalan, Kaveri Balan;Sigman, Matthew S.. And the article was included in Journal of the American Chemical Society in 2009.Formula: C6H12BrCl The following contents are mentioned in the article:

An unconventional route for the formation of sp³-sp³ C-C bonds from various styrenes and an organozinc reagent in a formal alkene hydroalkylation process is detailed. Mechanistically, this process is proposed to proceed by initial transmetalation followed by formation of a Pd-H species, which is subsequently trapped by the styrene. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Formula: C6H12BrCl).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Formula: C6H12BrCl

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Rational design and fabrication of an acid-resistant UZM-5 zeolite membrane for pervaporation dehydration processes was written by Yao, Rui;Peng, Yuan;Song, Hongling;Zhu, Chenyu;Wang, Pengyuan;Lun, Kun;Yang, Weishen. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2021.HPLC of Formula: 75-57-0 The following contents are mentioned in the article:

A UZM-5 zeolite membranes with pure UFI phase were fabricated using a charge d. mismatch-assisted tertiary growth approach. Taking full advantage of the suitable Si/Al ratio and pore size, the obtained zeolite membranes revealed an outstanding acid-resistant capacity and provided great potential for acetic acid pervaporation dehydration applications. This study involved multiple reactions and reactants, such as Tetramethylammonium chloride (cas: 75-57-0HPLC of Formula: 75-57-0).

Tetramethylammonium chloride (cas: 75-57-0) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.HPLC of Formula: 75-57-0

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Synthesis of 1-(arylsulfonyl)pyrrolidines from aryl alcohols and 1-[(4-chlorophenyl)sulfonyl]-2-ethoxypyrrolidine was written by Smolobochkin, A. V.;Anikina, E. A.;Gazizov, A. S.;Burilov, A. R.;Pudovik, M. A.. And the article was included in Russian Journal of Organic Chemistry in 2017.Electric Literature of C6H5ClO2 The following contents are mentioned in the article:

Acid-catalyzed reaction of 1-[(4-chlorophenyl)sulfonyl]-2-ethoxypyrrolidine with aryl alcs. led to the formation of new 1-(arylsulfonyl)pyrrolidines. The reaction proceeded under mild conditions and might be used as a convenient method for the synthesis of pyrrolidine-1-sulfonylarene derivatives containing a phenol fragment in the position 2. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Electric Literature of C6H5ClO2).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Electric Literature of C6H5ClO2

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Acid-Mediated C-N Bond Cleavage in 1-Sulfonylpyrrolidines: An Efficient Route towards Dibenzoxanthenes, Diarylmethanes, and Resorcinarenes was written by Gazizov, Almir S.;Smolobochkin, Andrey V.;Anikina, Ekaterina A.;Strelnik, Anna G.;Burilov, Alexander R.;Pudovik, Michail A.. And the article was included in Synlett in 2018.Synthetic Route of C6H5ClO2 The following contents are mentioned in the article:

The rare example of pyrrolidine C-N bond cleavage in 1-sulfonylpyrrolidines in acidic media in the presence of phenols is reported. The reaction proceeds under mild conditions and provides a convenient route to otherwise hardly accessible and previously unknown dibenzoxanthenes, diarylbutanes, and resorcinarenes having a sulfonylamide moiety. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Synthetic Route of C6H5ClO2).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).Synthetic Route of C6H5ClO2

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Microwave-Assisted Synthesis of d/l-Agrimonolide was written by Cui, Yu-Ang;Zhang, Guang-Yu;Li, Yun-Zhi;Li, Wei;Tanabe, Genzoh;Osamu, Muraoka;Xie, Wei-Jia. And the article was included in Asian Journal of Organic Chemistry in 2022.Application of 95-88-5 The following contents are mentioned in the article:

In this study, authors reported an improved approach for the synthesis of d/l Agrimonolide from 4-chlororesorcinol. It was found that a microwave assisted intramol. esterification is an effective way to construct the 3,4-dihydroisocoumarin core structure. The target d/l Agrimonolide is obtained in 7 steps with the overall yields of 20.7%. This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Application of 95-88-5).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Application of 95-88-5

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Facile synthesis of acacetin and its derivatives was written by Zhao, Yuan;Cai, Li;Sui, Qiang;Lin, Feng;Jiang, Wen;Chen, Jianli;Lu, Weigeng;Gao, Qi. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2016.Safety of 4-Chlororesorcinol The following contents are mentioned in the article:

Acacetin, an O-methylated bioflavonoid isolated from the traditional Chinese medicine Xuelianhua (Saussurea tridactyla), is a promising orally effective atrium-selective antiarrhythmic agent for the treatment of atrial fibrillation (AF). Here we describe an efficient two-component method for the synthesis of acacetin and its derivatives This study involved multiple reactions and reactants, such as 4-Chlororesorcinol (cas: 95-88-5Safety of 4-Chlororesorcinol).

4-Chlororesorcinol (cas: 95-88-5) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Safety of 4-Chlororesorcinol

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics