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Benzenesulfonothioic acid, 4-methyl-, S,S'-[1,2-phenylenebis(methylene)] ester, also known as 4-methylbenzenesulfonothioic acid S,S'-[1,2-phenylenebis(methylene)] ester, is a chemical compound with the molecular formula C15H14O2S3. It is a derivative of benzenesulfonothioic acid, featuring a 4-methyl group attached to the benzene ring and a 1,2-phenylenebis(methylene) bridge connecting two S,S'-benzenesulfonothioic acid moieties. Benzenesulfonothioic acid, 4-methyl-, S,S'-[1,2-phenylenebis(methylene)] ester is characterized by its unique structure, which consists of a benzene ring with a sulfonothioic acid group at the 4-position and a methylene-bridged phenylene linker connecting two such groups. It is an organic sulfur compound that may have applications in the synthesis of various chemical products, such as dyes, pharmaceuticals, or other specialty chemicals, due to its specific reactivity and functional groups.

1855-05-6

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1855-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1855-05-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,5 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1855-05:
(6*1)+(5*8)+(4*5)+(3*5)+(2*0)+(1*5)=86
86 % 10 = 6
So 1855-05-6 is a valid CAS Registry Number.

1855-05-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Bis(p-tolylsulfonylthiomethyl)benzene

1.2 Other means of identification

Product number -
Other names α,α'-Bis-p-toluolsulfonylthio-o-xylol

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:1855-05-6 SDS

1855-05-6Relevant academic research and scientific papers

Organic Disulfides and Related Substances. 47. Some Novel Types of Aminoalkyl Disulfides

Singh, Pramod K.,Field, Lamar

, p. 67 - 68 (2007/10/02)

Several novel types of amino disulfides are reported, together with their stabilities in D2O (i.e., resistance to disproportionation).These disulfides contain the group H2N(CH2)2, known to be radioprotective, as an R group in alkenyl and arylene systems of the structure RSSCH2-C.=C.-CH2SSR.The disulfides (5-7) were synthesized by reactions of 2-aminoethanethiol with novel thiosulfonates (1-3).

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