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4-Nitrobenzenesulfonothioic acid S-phenyl ester is an organic compound with the chemical formula C12H9NO4S2. It is a derivative of benzenesulfonothioic acid, featuring a nitro group at the para position and a phenyl group attached to the sulfur atom through an ester linkage. This yellow crystalline solid is soluble in organic solvents and has a molecular weight of 297.34 g/mol. The compound is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. Due to its reactivity and potential applications, it is essential to handle 4-Nitrobenzenesulfonothioic acid S-phenyl ester with care, following proper safety protocols.

3660-41-1

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3660-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3660-41-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,6 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3660-41:
(6*3)+(5*6)+(4*6)+(3*0)+(2*4)+(1*1)=81
81 % 10 = 1
So 3660-41-1 is a valid CAS Registry Number.

3660-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitro-benzenethiosulfonic acid S-phenyl ester

1.2 Other means of identification

Product number -
Other names 4-Nitro-benzenethiosulfonic acid S-phenyl ester

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:3660-41-1 SDS

3660-41-1Downstream Products

3660-41-1Relevant academic research and scientific papers

Ammonium iodide-mediated electrosynthesis of unsymmetrical thiosulfonates from arenesulfonohydrazides and thiols

Terent'ev, Alexander O.,Mulina, Olga M.,Ilovaisky, Alexey I.,Kokorekin, Vladimir A.,Nikishin, Gennady I.

, p. 80 - 82 (2019/02/20)

Unsymmetrical thiosulfonates were synthesized from thiols and arenesulfonohydrazides by their electrolysis in undivided cell equipped with graphite anode and stainless steel cathode under high current density applying NH4I both as a redox catal

H2O2-mediated metal-free protocol towards unsymmetrical thiosulfonates from sulfonyl hydrazides and disulfides in PEG-400

Peng, Zhihong,Zheng, Xiao,Zhang, Yingjun,An, Delie,Dong, Wanrong

supporting information, p. 1760 - 1764 (2018/04/30)

A green and practical protocol between sulfonyl hydrazides and disulfides is herein reported for the synthesis of unsymmetrical thiosulfonates with the assistance of H2O2 in PEG-400, releasing N2 and H2O as the byproducts. The efficient and compatible process was considered to take place in the absence of metallic catalysts through a radical mechanism as determined by EPR analysis.

Copper-Catalyzed TBHP-Mediated Radical Cross-Coupling Reaction of Sulfonylhydrazides with Thiols Leading to Thiosulfonates

Zhang, Guo-Yu,Lv, Shuai-Shuai,Shoberu, Adedamola,Zou, Jian-Ping

, p. 9801 - 9807 (2017/09/22)

A tert-butyl hydroperoxide (TBHP)-mediated coupling of sulfonylhydrazides with thiols catalyzed by CuBr2 to afford thiosulfonates via a radical process is described.

INVESTIGATION OF THIOSULFONIC ACIDS. XXXIV. REACTION OF THIOSULFONIC ESTERS WITH SULFENAMIDES

Boldyrev, B. G.,Bilozor, T. K.

, p. 1669 - 1671 (2007/10/02)

Thiosulfonic esters react with sulfenamides to form different thiosulfonic esters and sulfenamides.The process is only realized with initial esters having high reactivity and amides having high nucleophilicity, both significantly higher than the analogous characteristics of the final products.

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