Tag: M.W=100-150

Shen, ZW; Meng, DD; Imran, S; Yan, CH; Sun, HM in [Shen, Zheng-Wang; Meng, Die-Die; Imran, Sajid; Sun, Hong-Mei] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Key Lab Organ Synth Jiangsu Prov, Suzhou 215123, Jiangsu, Peoples R China; [Yan, Chun-Hui] Soochow Univ, Anal & Testing Ctr, Suzhou 215123, Jiangsu, Peoples R China published Heteroleptic Ni(II) Complexes Bearing a Bulky Yet Flexible IBiox-6 Ligand: Improved Selectivity in Cross-Electrophile Coupling of Benzyl Chlorides with Aryl Chlorides/Fluorides in 2020.0, Cited 37.0. Category: chlorides-buliding-blocks. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8.

A bisoxazoline-derived NHC known as IBiox-6 reacted smoothly with Ni[P(OEt)(3)](2)Br-2 and Ni(PPh3)(2)Br-2 to give the respective heteroleptic Ni(II) complexes Ni(IBiox-6)[P(OEt)(3)]Br-2 (1) and Ni(IBiox-6)(PPh3)Br-2 (2) in yields of 60% and 71%. Their crystal structures were characterized to reveal a rare cis disposition of the IBiox-6 ligand to the phosphite ligand in 1, while 2 possessed the more common trans configuration. Both complexes catalyzed the cross-electrophile coupling of benzyl chlorides with aryl chlorides and fluorides in the presence of Mg turnings at 50 degrees C via a real one-pot procedure, featuring no requirement for temperature variation or portionwise addition of any coupling partner. In particular, complex 1 showed a better balance between the catalytic activity and selectivity. The scope of the procedure catalyzed by 1 and Mg turnings was investigated, providing a highly selective, simple, and practical approach to the synthesis of diarylmethanes with high steric hindrance and various functional groups, including oligo-diarylmethane with asymmetric structures.

About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Shen, ZW; Meng, DD; Imran, S; Yan, CH; Sun, HM or concate me.. Category: chlorides-buliding-blocks

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

An article Distribution characteristics and ecological evaluation of chlorobenzene compounds in surface sediment of the Maowei Sea, Guangxi, China WOS:000465957500001 published article about POLYCHLORINATED-BIPHENYLS PCBS; POLYBROMINATED DIPHENYL ETHERS; AROMATIC-HYDROCARBONS PAHS; DIBENZO-P-DIOXINS; SPATIAL-DISTRIBUTION; MARINE FISH; ESTUARY; TRENDS; PBDES; WATER in [Liao, Riquan; Kang, Zhenjun; Yang, Bin] Beibu Gulf Univ, Guangxi Key Lab Beibu Gulf Marine Biodivers Conse, Qinzhou 535000, Guangxi, Peoples R China; [Li, Weitao; Wang, Liang] Shanghai Univ, Inst Nanochem & Nanobiol, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China; [Tang, Liang] Shanghai Univ, Shanghai Inst Appl Radiat, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China in 2019.0, Cited 28.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8. Product Details of 95-49-8

To enhance our understanding on environmental conditions of the Maowei Sea in Guangxi province, China, the concentration and distribution of 22 chlorobenzene compounds (CBs) in the surface sediment were determined by gas chromatography-mass spectrometry (GC-MS). The relationship of the sediment between CBs and total organic carbon (TOC) was also investigated. The results showed that a total of eight kinds of CBs compounds were detected in the sediment samples which were collected from the coastal environment of the Maowei Sea, with an average concentration of 15.3ngg(-1) (the concentration range, 2.5-61.5ngg(-1)). The rank of their average concentrations was as follows: 2,3,4,5,6-pentachlorotoluene>hexachlorobenzene, 2-chlorotoluene, 3-chlorotoluene and 2,3-dichlorotoluene>2,4-dichlorotoluene>4-chlorotoluene>pentachlorobenzene. Most CBs were distributed in sediments along the east coast of the Maowei Sea. For total TOC content in sediments, the concentration in the sampling locations was similar, with a mean concentration of 8.83gkg(-1) (the concentration range, 4.87-20.13gkg(-1)). However, there was no significant correlation between the concentration of TOC and total CBs. Compared to the corresponding CBs in the sediment of other coastal areas in mainland China and other countries, the value of CBs in the Maowei Sea was low.

About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Liao, RQ; Li, WT; Kang, ZJ; Tang, L; Yang, B; Wang, L or concate me.. Product Details of 95-49-8

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

I found the field of Chemistry very interesting. Saw the article LiCl-Accelerated Multimetallic Cross-Coupling of Aryl Chlorides with Aryl Triflates published in 2019.0. Product Details of 95-49-8, Reprint Addresses Weix, DJ (corresponding author), Univ Wisconsin, Madison, WI 53706 USA.. The CAS is 95-49-8. Through research, I have a further understanding and discovery of 1-Chloro-2-methylbenzene

While the synthesis of biaryls has advanced rapidly in the past decades, cross-Ullman couplings of aryl chlorides, the most abundant aryl electrophiles, have remained elusive. Reported here is the first general cross-Ullman coupling of aryl chlorides with aryl triflates. The selectivity challenge associated with coupling an inert electrophile with a reactive one is overcome using a multimetallic strategy with the appropriate choice of additive. Studies demonstrate that LiCl is essential for effective cross-coupling by accelerating the reduction of Ni(II) to Ni(0) and counteracting autoinhibition of reduction at Zn(0) by Zn(II) salts. The modified conditions tolerate a variety of functional groups on either coupling partner (42 examples), and examples include a three-step synthesis of flurbiprofen.

Product Details of 95-49-8. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Huang, LB; Ackerman, LKG; Kang, K; Parsons, AM; Weix, DJ or concate me.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

I found the field of Environmental Sciences & Ecology; Public, Environmental & Occupational Health very interesting. Saw the article Distribution Characteristics of Volatile Organic Compounds and Contribution to Ozone Formation in a Coking Wastewater Treatment Plant published in 2020.0. Formula: C7H7Cl, Reprint Addresses Wei, CH (corresponding author), South China Univ Technol, Sch Environm & Energy, Minist Educ, Key Lab Pollut Control & Ecosyst Restorat Ind Clu, Guangzhou 510006, Peoples R China.. The CAS is 95-49-8. Through research, I have a further understanding and discovery of 1-Chloro-2-methylbenzene

Ozone pollution, which can be caused by photochemical reactions, has become a serious problem. The ozone formation potential (OFP) is used to describe the photochemical reactivity. Volatile organic compounds (VOCs) are main precursors of ozone formation, and wastewater treatment plants (WWTPs) are important sources of VOCs. Therefore, it is necessary to study the concentration level and OFP of VOCs from WWTPs. In this work, a coking WWTP with anaerobic-oxic-oxic (A/O/O) processes in Shaoguan city, Guangdong province, China, was selected to investigate the characteristics of VOCs at wastewater treatment areas and office areas. The OFP of VOCs was estimated by the maximum incremental reactivity (MIR) coefficient method. Results showed that 17 VOCs were detected, and the total concentration of VOCs was the highest at the raw water tank (857.86 mu g m(-3)). The benzene series accounted for 69.0%-86.9% and was the main component of VOCs in the WWTP. Based on OFP data, the top six VOCs contributing most to the OFP were m-xylene, toluene, p-xylene, o-xylene, styrene, and benzene. This study provides field data and information on the environmental risk of VOCs for coking companies and environmental departments. We found that the priority control sources of VOCs were wastewater treatment units because of their larger OFP contributions.

Formula: C7H7Cl. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Zhang, YX; Zang, TT; Yan, B; Wei, CH or concate me.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Authors Chang, RK; Clairmont, BP; Lin, S; MacArthur, AHR in AMER CHEMICAL SOC published article about N-ARYLATION; (HETERO)ARYL CHLORIDES; HALIDES; LIGANDS; AMIDES; LACTAMS in [Chang, Raymond K.; Clairmont, Brice P.; Lin, Shirley; MacArthur, Amy H. Roy] US Naval Acad, Dept Chem, 572 Holloway Rd, Annapolis, MD 21402 USA in 2019.0, Cited 34.0. Application In Synthesis of 1-Chloro-2-methylbenzene. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8

A concurrent tandem catalytic (CTC) methodology has been developed for the amidation of aryl chlorides where the aryl chloride is first converted to an aryl iodide via halogen exchange and the aryl iodide is subsequently transformed into the aryl amide. A variety of aryl chlorides were converted to aryl amides in up to 85% isolated yield using 20 mol % CuI, 60 mol % N,N’-cyclohexane-1,2-diamine, 2.2 equiv of K2CO3, and 1.05-1.5 equiv of amide in acetonitrile at 200 degrees C after 0.75-1 h. The same copper/ligand system served as multifunctional catalyst for both steps of the concurrent catalytic process with iodide present in substoichiometric amounts. Mechanistic studies were consistent with CTC amidation occurring via a nonradical mechanism. Kinetic modeling was conducted to investigate the effect of competitive direct amidation of an aryl chloride or aryl bromide on the formation of product over time during a CTC amidation reaction.

Application In Synthesis of 1-Chloro-2-methylbenzene. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Chang, RK; Clairmont, BP; Lin, S; MacArthur, AHR or concate me.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Quality Control of 1-Chloro-2-methylbenzene. In 2020.0 J MOL STRUCT published article about ALUMINUM; ELECTRODEPOSITION; CHLORIDE in [Sakhalkar, Mangesh; Pradhan, Jeevan; Chandra, Sudeshna] SVKMs NMIMS Deemed Be Univ, Sunandan Divatia Sch Sci, Dept Chem, VL Mehta Rd, Mumbai 400056, Maharashtra, India; [Sakhalkar, Mangesh; Choudhury, Rudra Prosad; Bhakthavatsalam, Vishnupriya; Lande, Sharad, V] Ms Reliance Ind Ltd, TC30C,First Floor,Reliance Corp Pk, Ghansoli 400701, Navi Mumbai, India in 2020.0, Cited 39.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8.

Chloroaluminate ionic liquids (ILs) have been immensely used as homogeneous catalyst in Friedel-Crafts reaction. We have recently synthesized chloroaluminate ILs by reacting aluminium chloride with a hydrophobic neutral ligand i.e. tributylamine (TBA:AlCl3). The current study elaborates on the investigations of the composition of the ionic liquids at various stages of their formation. The ionic liquids were synthesized using various mole ratios of tributyl amine and aluminium chloride in range of 1:1 to 1:2.3, in presence of an aromatic solvent in a one pot reaction. Various characterization techniques like Mass spectrometry, Al-27 Nuclear Magnetic Resonance, P-31 Nuclear Magnetic Resonance and Fourier Transform Infrared spectroscopy were used to elucidate the formation of various moieties of the TBA:AlCl3 Ionic Liquid. This study also elaborates on the investigations of the cationic and anionic moieties and their structure-property relationship for various applications. Various Friedel-Crafts reaction of industrial importance were performed using the ionic liquid having (Al2Cl7)(-) moiety to assess its performance and compared with conventional processes. The synthesized products were characterised by sophisticated analytical techniques like H-1 NMR, C-13 NMR, FTIR, GC-MS, GC-FID, to name a few. This class of ionic liquids also have importance in various electrochemical applications like aluminium deposition and aluminium batteries. (C) 2020 Elsevier B.V. All rights reserved.

Quality Control of 1-Chloro-2-methylbenzene. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Sakhalkar, M; Choudhury, RP; Bhakthavatsalam, V; Lande, SV; Pradhan, J; Chandra, S or concate me.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Authors Sinai, A; Simko, DC; Szabo, F; Paczal, A; Gati, T; Benyei, A; Novak, Z; Kotschy, A in WILEY-V C H VERLAG GMBH published article about SUZUKI-MIYAURA; N-TOSYLHYDRAZONES; ROOM-TEMPERATURE; HOMOGENEOUS CATALYSTS; CHLORIDES; SONOGASHIRA; AMINATION; HALIDES; LIBRARIES; ARYLATION in [Sinai, Adam; Paczal, Attila; Gati, Tamas; Kotschy, Andras] Servier Res Inst Med Chem, Zahony Utca 7, H-1031 Budapest, Hungary; [Sinai, Adam; Simko, Daniel Cs.; Szabo, Fruzsina; Novak, Zoltan] Eotvos Lorand Univ, Inst Chem, ELTE Lendulet Catalysis & Organ Synth Res Grp, Pazmany Peter Stny 1-A, H-1117 Budapest, Hungary; [Benyei, Attila] Univ Debrecen, Dept Pharmaceut Chem, Egyet Ter 1, H-4032 Debrecen, Hungary in 2020.0, Cited 72.0. Safety of 1-Chloro-2-methylbenzene. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8

Synthesis, temperature-dependent NMR structure investigation and utilization of a new, stable and easily accessible aryl-diadamantylphosphine ligand family is reported. The bulky and electron-rich phosphorus center of the ligand enhances the catalytic activity of palladium in cross-coupling reactions of sterically demanding ortho-substituted aryl halides. In our study, we demonstrated the synthetic applicability of the new phosphine ligands in Buchwald-Hartwig and tosyl hydrazone coupling reactions.

Safety of 1-Chloro-2-methylbenzene. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Sinai, A; Simko, DC; Szabo, F; Paczal, A; Gati, T; Benyei, A; Novak, Z; Kotschy, A or concate me.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

In 2020.0 GREEN CHEM published article about ONE-POT SYNTHESIS; CARBONYL; REDUCTION; AMINATION; CLUSTERS in [Srivastava, Avinash K.; Sharma, Charu; Joshi, Raj K.] Malaviya Natl Inst Technol, Dept Chem, Jaipur 302017, Rajasthan, India in 2020.0, Cited 34.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8. Safety of 1-Chloro-2-methylbenzene

A strategy involving bimetallic catalysis with a combination of Cp*Co(CO)I-2 and Cu(OAc)(2) was used for performing Buchwald-type C-N coupling reactions of aryl chlorides with amines. The reactions proceeded at 100 degrees C to produce excellent yields of many of the desired C-N coupled products, in 4 h, under aerobic reaction conditions. The reactions were shown to run under base-free and solvent-free conditions, enabling this strategy to work efficiently for electron-withdrawing and base-sensitive functionalities. The presented methodology was found to be equally efficient for electron-donating functionalities as well as for primary (1 degrees) and secondary (2 degrees) aromatic and aliphatic amines. Moreover, the products were easily separated through the extractions of the organic aqueous layer, with this process chromatographic separations is not required.

About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Srivastava, AK; Sharma, C; Joshi, RK or concate me.. Safety of 1-Chloro-2-methylbenzene

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Application In Synthesis of 1-Chloro-2-methylbenzene. Dandia, A; Mahawar, DK; Sharma, R; Badgoti, RS; Rathore, KS; Parewa, V in [Dandia, Anshu; Mahawar, Dinesh Kumar; Sharma, Ruchi; Badgoti, Ranveer Singh; Parewa, Vijay] Univ Rajasthan, Ctr Adv Studies, Dept Chem, Jaipur, Rajasthan, India; [Rathore, Kuldeep S.] Arya Coll Engn & IT, Dept Phys, Jaipur, Rajasthan, India published Graphene oxide-catalyzed C-Sp3-H activation of methylarenes in aqueous medium: A unified metal-free access to amides and benzimidazoles in 2019.0, Cited 54.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8.

Graphene oxide (GO)-catalyzed selective synthesis of amides via C-Sp3-H activation of methylarenes and consequent C-N bond formation with anilines under aqueous medium has been described. Oxygen functionality allied with GO surface played a dual role both as acid catalyst and oxidizing agent to some extent. However, GO has a copious effect on the reaction, shown by a high TOF value with TBHP as co-oxidant. The decisive role of carboxylic acid functional groups on GO nanosheets in this metal-free strategy has been confirmed and was monitored by various analytic techniques viz. Fourier transform-infrared, UV-Vis, Raman and XPS. A plausible mechanism was proposed by control experiments and by the isolation of the intermediate. Over-oxidation of methylarenes was not detected, and high recyclability of the carbocatalyst with its heterogeneous behavior facilitated the isolation and purification of the desired products. We have further explored the utility of this process for the chemoselective synthesis of benzimidazoles.

Application In Synthesis of 1-Chloro-2-methylbenzene. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Dandia, A; Mahawar, DK; Sharma, R; Badgoti, RS; Rathore, KS; Parewa, V or concate me.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

I found the field of Science & Technology – Other Topics; Energy & Fuels very interesting. Saw the article Study on the influence of small molecular gases on toluene reforming in molten salt published in 2020.0. Name: 1-Chloro-2-methylbenzene, Reprint Addresses Hu, HY (corresponding author), Huazhong Univ Sci & Technol, Sch Energy & Power Engn, State Key Lab Coal Combust, Wuhan 430074, Peoples R China.. The CAS is 95-49-8. Through research, I have a further understanding and discovery of 1-Chloro-2-methylbenzene

The upgrading of tar is a key issue for the sufficient application of biowaste pyrolysis technology. Molten salt, with high migration and diffusion of ions to prevent the deactivation of coke deposition of tar reforming functional metals, is considered as a feasible catalytic reaction medium and heat carrier for the upgrading of tar. The present study investigated the interactions between small molecular pyrolysis gases (including H-2, CO, CH4) and main tar model compound in ternary carbonate eutectics (Li2CO3-Na2CO3-K2CO3). The results demonstrated that H-2 could be decomposed to produce H radicals, promoting the conversion of toluene into gaseous products. CO32- could consume H radicals required by toluene cracking, making the process toluene polymerized to polycyclic aromatic hydrocarbons be strengthened. On the other hand, CO would react with OH radicals to produce H radicals and could enhance gas-generating process. In addition, toluene could react with CO to form benzaldehyde and phenylacetaldehyde. With the addition of CH4, more H radicals were supposed to be consumed, and toluene cracking process was further inhibited. Finally, the effect sequence of small molecular gases (H-2 > CH4 > CO) on toluene reforming reaction was authenticated by investigating the impacts of introducing any two gases in toluene reforming. (C) 2020 Elsevier Ltd. All rights reserved.

About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Yang, F; Hu, HY; Gao, Q; Yang, YH; Tang, H; Xie, K; Liu, H; He, Y; Yao, H or concate me.. Name: 1-Chloro-2-methylbenzene

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics