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2,4-Dinitro-1-[(phenylmethyl)thio]benzene is an organic compound with the chemical formula C13H10N2O4S. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. 2,4-Dinitro-1-[(phenylmethyl)thio]benzene is characterized by the presence of two nitro groups (NO2) at the 2nd and 4th positions of the benzene ring, a phenylmethyl (benzyl) group attached to the sulfur atom, and a thiol (SH) group. It is used as an intermediate in the synthesis of various chemical compounds and has potential applications in the pharmaceutical and agrochemical industries. Due to its chemical structure, it may exhibit toxic properties and should be handled with care.

7343-61-5

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7343-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7343-61-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,4 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7343-61:
(6*7)+(5*3)+(4*4)+(3*3)+(2*6)+(1*1)=95
95 % 10 = 5
So 7343-61-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2O4S/c16-14(17)11-6-7-13(12(8-11)15(18)19)20-9-10-4-2-1-3-5-10/h1-8H,9H2

7343-61-5SDS

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 2,4-Dinitro-1-[(phenylmethyl)thio]benzene

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

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More Details:7343-61-5 SDS

7343-61-5Relevant 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

supporting information, p. 724 - 727 (2013/02/25)

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.

Co-C bond cleavage in the reactions of alkyl, benzyl and heteroaromaticmethyl cobaloximes with arene sulfenyl chloride: Homolytic and heterolytic pathways

Gupta,Dixit, Vandana,Das, Indira

, p. 49 - 58 (2007/10/03)

The reactions of arene sulfenyl chlorides, ArSCl, (Ar=Ph, C6Cl5, 2,4 (NO2)2C6H3) with organocobaloximes, RCo(dmgH)2Py, (R=alkyl, benzyl and heteroaromaticmethyl) were carried out under thermal and photochemical conditions. A variety of organic and organometallic products are formed depending upon the substrate cobaloxime. For 3-methoxybenzyl and heteroaromaticmethyl cobaloximes the results suggest that they represent a unique class of cobaloximes whereby both the aromatic ring as well as the Co-C bond are highly activated towards attack by the arene sulfenyl chloride. Both homolytic as well as heterolytic pathways are operative.

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