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349-33-7

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349-33-7 Usage

General Description

AKOS B018302, also known as 2-chloro-5-nitrobenzaldehyde, is a chemical compound with the molecular formula C7H4ClNO3. It is a yellow crystalline solid commonly used in the synthesis of various pharmaceuticals, agrochemicals, and dyes. AKOS B018302 is a potent antimicrobial agent and is also used as an intermediate in the manufacturing of drugs. AKOS B018302 is known for its toxic and irritating properties and should be handled with caution. It is important to follow safety guidelines and regulations when working with this chemical to prevent any harm to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 349-33-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 349-33:
(5*3)+(4*4)+(3*9)+(2*3)+(1*3)=67
67 % 10 = 7
So 349-33-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H6FNOS2/c11-7-3-1-2-6(4-7)5-8-9(13)12-10(14)15-8/h1-5H,(H,12,13,14)/b8-5+

349-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (5Z)-5-(3-fluorobenzylidene)-2-thioxo-1,3-thiazolidin-4-one

1.2 Other means of identification

Product number -
Other names -

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:349-33-7 SDS

349-33-7Relevant articles and documents

A facile synthesis of (Z)-5-(substituted)-2-(methylthio)thiazol-4(5H)-one using microwave irradiation and conventional method

Pansare, Dattatraya N.,Shinde, Devanand B.

supporting information, p. 1107 - 1110 (2014/02/14)

A new effective approach to the synthesis of some new (Z)-5-(substituted)- 2-thioxothiazolidin-4-one 3a-l and (Z)-5-(substituted)-2-(methylthio)thiazol- 4(5H)-one 5a-l is reported under microwave irradiation as well as conventional conditions.

Synthesis and characterization of (Z)-5-arylmethylidenerhodanines with photosynthesis-inhibiting properties

Opletalova, Veronika,Dolezel, Jan,Kralova, Katarina,Pesko, Matus,Kunes, Jiri,Jampilek, Josef

experimental part, p. 5207 - 5227 (2011/08/06)

A series of rhodanine derivatives was prepared. The synthetic approach, analytical and spectroscopic data of all synthesized compounds are presented. Lipophilicity of all the discussed rhodanine derivatives was analyzed using the RP-HPLC method. The compo

Selective small molecule inhibitors of the potential breast cancer marker, human arylamine N-acetyltransferase 1, and its murine homologue, mouse arylamine N-acetyltransferase 2

Russell, Angela J.,Westwood, Isaac M.,Crawford, Matthew H.J.,Robinson, James,Kawamura, Akane,Redfield, Christina,Laurieri, Nicola,Lowe, Edward D.,Davies, Stephen G.,Sim, Edith

experimental part, p. 905 - 918 (2009/09/25)

The identification, synthesis and evaluation of a series of rhodanine and thiazolidin-2,4-dione derivatives as selective inhibitors of human arylamine N-acetyltransferase 1 and mouse arylamine N-acetyltransferase 2 is described. The most potent inhibitors

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