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Ethanethioic acid, S-[2-(chlorocarbonyl)phenyl] ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62972-22-9

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62972-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62972-22-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,7 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62972-22:
(7*6)+(6*2)+(5*9)+(4*7)+(3*2)+(2*2)+(1*2)=139
139 % 10 = 9
So 62972-22-9 is a valid CAS Registry Number.

62972-22-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name S-(2-carbonochloridoylphenyl) ethanethioate

1.2 Other means of identification

Product number -
Other names Acetylthiosalicylsaeurechlorid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62972-22-9 SDS

62972-22-9Relevant academic research and scientific papers

Efficient synthesis of 2-alkylidene-4h-3,1-benzoxathiin-4-ones and determination of their double bond configuration

Shimizu, Masao,Yamanaka, Masaki,Ando, Wataru,Shimada, Shigeru,Konakahara, Takeo,Sakai, Norio

, p. 981 - 993 (2014/04/17)

2-Alkylidene-4H-3,1-benzoxathiin-4-ones were efficiently synthesized by reaction of 2-(acylthio)benzoic acids with condensation reagents in the presence of base. The E and Z isomers of the products were distinguished by comparison of the chemical shifts o

Synthesis and characterization of an anticoagulant 4-hydroxy-1-thiocoumarin by FTIR, FT-Raman, NMR, DFT, NBO and HOMO-LUMO analysis

Arjunan,Santhanam,Sakiladevi,Marchewka,Mohan

, p. 305 - 316 (2013/05/09)

Experimental and theoretical investigations on the molecular structural, electronic and the vibrational characteristics of 4-hydroxy-1-thiocoumarin are presented. Conformational analysis was carried out to obtain the more stable configuration of the compo

New nuclear transcription factors regulators

-

Page/Page column 5-6, (2008/06/13)

The present invention relates to novel compounds that are nuclear transcription factors (NTF) regulators. The present invention also provides methods for treating, preventing and/or reducing inflammation-associated diseases by regulating NTF in the cardiovascular, connective tissue, pulmonary, gastrointestinal, respiratory, urogenital, nervous, or cutaneous systems as well as tumoral and infective diseases employing said compounds. The present invention is based on the discovery that it is possible to link regulators of NTF to a pharmacologically active compound helpful for treating disorders in the cardiovascular, connective tissue, pulmonary, gastrointestinal, respiratory, urogenital, nervous, or cutaneous systems or tumoral and infective diseases. The resulting compounds have good bioavailability, increased activity and/or safety.

Efficient and practical syntheses of benzothiopyran derivatives

Jung, Jae-Chul,Kim, Ju-Cheun,Park, Oee-Sook

, p. 1193 - 1203 (2007/10/03)

Concise and inexpensive methods for the preparation of 4-hydroxy-1- thiocoumarin and 2-methylthiochromone from 2-mercaptobenzoic acid are described, which should be readily amenable to large scale synthesis.

Aspects of Tautomerism: Part X - Neighbouring Group Effects on the Structure and Reactivity Patterns of Acid Chlorides

Bhatt, M. Vivekananda,El Ashry, Shaker H.,Somayaji, Vishwanatha

, p. 473 - 486 (2007/10/02)

The influence of neighbouring groups on the structure and reactivity patterns of over one hundred acid chlorides derived from γ- and δ-keto acids, 1,2- and 1,3-dicarboxylic acid half-esters and diacid chlorides have been examined.Contrary to reports in the literature, text books and monographs, evidence has been obtained for the non-existence of tautomerism between the isomeric pairs of either acid chlorides or half-ester acid chlorides.ce.

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