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Benzenesulfonamide, N-hydroxy-4-methyl-N-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88978-52-3

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88978-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88978-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,7 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88978-52:
(7*8)+(6*8)+(5*9)+(4*7)+(3*8)+(2*5)+(1*2)=213
213 % 10 = 3
So 88978-52-3 is a valid CAS Registry Number.

88978-52-3SDS

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 N-hydroxy-4-methyl-N-(trifluoromethyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-trifluoromethyl-N-hydroxy-p-toluenesulfonamide

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:88978-52-3 SDS

88978-52-3Downstream Products

88978-52-3Relevant academic research and scientific papers

Reaction of Trifluoronitrosomethane with Arenesulfonohydrazides. Synthesis of N-Trifluoromethyl-N-hydroxyarenesulfonamides

Sekiya, Akira,Umemoto, Teruo

, p. 2962 - 2964 (2007/10/02)

The reaction of trifluoronitrosomethane 1 with arenesulfonohydrazides resulted in the formation of N-trifluoromethyl-N-hydroxyarenesulfonamides 3 which were characterized by spectral and elemental analyses.It showed a sharp contrast to the reaction of 1 with acyl- or carbamoylhydrazines, which afforded the corresponding trifluoromethylazo compounds.As an alternative route, 3 could be synthesized by the reaction of 1 with arenesulfinic acids or their salts.The sulfonamides 3 were converted to the corresponding methyl ethers or tosylates.

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