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

349-33-7

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349-33-7 Usage

Uses

Used in Pharmaceutical Industry:
AKOS B018302 is used as an intermediate in the synthesis of various pharmaceuticals for its antimicrobial properties, contributing to the development of new drugs and treatments.
Used in Agrochemical Industry:
AKOS B018302 is used as an intermediate in the production of agrochemicals, where its antimicrobial properties can be harnessed to protect crops and enhance agricultural productivity.
Used in Dye Industry:
AKOS B018302 is used as a starting material in the synthesis of various dyes, taking advantage of its yellow crystalline solid form to create a range of colorants for different applications.
Used in Research and Development:
AKOS B018302 is utilized in research and development settings to explore its potential applications and properties further, including its antimicrobial activity and its role as a chemical intermediate in various chemical reactions.

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 academic research and scientific papers

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.

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.

, p. 1107 - 1110 (2015/02/19)

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

Practical one-pot two-step protocol for the microwave-assisted synthesis of highly functionalized rhodanine derivatives

Radi, Marco,Botta, Lorenzo,Casaluce, Gianni,Bernardini, Martina,Botta, Maurizio

experimental part, p. 200 - 205 (2010/10/19)

A fast and efficient protocol for the generation of substituted 5-arylidene rhodanines in a sequential one-pot two-step process combining the "Holmberg method" and the Knoevenagel condensation under microwaveassisted conditions has been developed. The final compounds 11a-k have been obtained in high yield and purity after a simple precipitation from, methanol, making this procedure facile, practical, and rapid to execute.

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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