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o-Chlormercapto-benzoesaeureaethylester, also known as 2-chloromercapto-benzoic acid ethyl ester, is an organic compound with the chemical formula C9H9ClO2S. It is a colorless to pale yellow liquid with a molecular weight of 214.68 g/mol. o-Chlormercapto-benzoesaeureaethylester is characterized by the presence of a chloromercapto group (-ClSH) attached to the ortho position of a benzoic acid molecule, which is further esterified with ethanol to form an ethyl ester. o-Chlormercapto-benzoesaeureaethylester is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the production of dyes and pigments. Due to its reactivity, it is essential to handle o-Chlormercapto-benzoesaeureaethylester with care, following proper safety protocols to minimize exposure and potential health risks.

1441-80-1

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1441-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1441-80-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,4 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1441-80:
(6*1)+(5*4)+(4*4)+(3*1)+(2*8)+(1*0)=61
61 % 10 = 1
So 1441-80-1 is a valid CAS Registry Number.

1441-80-1Relevant academic research and scientific papers

Synthesis and evaluation of novel sulfenamides as novel anti Methicillin-resistant Staphylococcus aureus agents

Shang, Jian-Li,Guo, Hui,Li, Zai-Shun,Ren, Biao,Li, Zheng-Ming,Dai, Huan-Qin,Zhang, Li-Xin,Wang, Jian-Guo

, p. 724 - 727 (2013)

A total of 29 novel sulfenamide compounds were synthesized, spectroscopically characterized and evaluated in vitro for antimicrobial activity against various infectious pathogens. Compounds 1b and 2c exhibited potent inhibition against clinical Methicillin-resistant Staphylococcus aureus (MRSA) strains with minimum inhibitory concentration (MIC) values of 1.56 μg/mL.

Synthesis and biological evaluation of nonsymmetrical aromatic disulfides as novel inhibitors of acetohydroxyacid synthase

Li, Zai-Shun,Wang, Wei-Min,Lu, Wei,Niu, Cong-Wei,Li, Yong-Hong,Li, Zheng-Ming,Wang, Jian-Guo

, p. 3723 - 3727 (2013/07/25)

46 Novel nonsymmetrical aromatic disulfides containing [1,3,4]thiadiazole or [1,3,4]oxadiazole groups were synthesized and their biological activities were evaluated as inhibitors of acetohydroxyacid synthase (AHAS, EC 2.2.1.6). Besides their strong in vitro inhibition against plant AHAS, compounds 3e and 3f also display 80-100% post-emergence herbicidal activities in greenhouse bioassay at 1500 g/ha dosage. The assay of exogenous branched-chain amino acids supplementation on rape root growth of 3e suggests that the herbicidal activity has relationship with AHAS inhibition.

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