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N-2-methoxycarbonylphenylthio-2-methoxycarbonylbenzenesulfenamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55255-14-6

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55255-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55255-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,5 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55255-14:
(7*5)+(6*5)+(5*2)+(4*5)+(3*5)+(2*1)+(1*4)=116
116 % 10 = 6
So 55255-14-6 is a valid CAS Registry Number.

55255-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-2-methoxycarbonylphenylthio-2-methoxycarbonylbenzenesulfenamide

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:55255-14-6 SDS

55255-14-6Downstream Products

55255-14-6Relevant academic research and scientific papers

Efficient synthesis of N-acylarenesulfenamides by acylation of arenesulfenamides

Bao, Ming,Shimizu, Masao,Shimada, Shigeru,Tanaka, Masato

, p. 303 - 309 (2007/10/03)

Acylation of arenesulfenamides proceeds efficiently by using either perfluorocarboxylic anhydrides or acid chlorides in the presence of pyridine as a base at low temperatures to give N-acylarenesulfenamides. Some N-alkylcarbonyl derivatives exist with imidic acid tautomers in an aprotic solvent.

A facile synthesis of 1,2-benzisothiazolin-3-ones from thiosalicylates

Shimizu, Masao,Kikumoto, Hisashi,Konakahara, Takeo,Gama, Yasuo,Shibuya, Isao

, p. 3005 - 3012 (2007/10/03)

Synthesis of 1,2-benzisothiazolin-3-ones by cyclization of 2- sulfenamoylbenzoates, which were prepared from amination of thiosalicylates by hydroxylamine-O-sulfonic acid, was examined. Although treatment of methyl 2-sulfenamoylbenzoate on heating gave unexpected 2-(2- methoxycarbonylphenylthio)-1,2-benzisothiazolin-3-one, the treatment with base at room temperature afforded 1,2-benzisothiazolin-3-one in a good yield.

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