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146533-54-2

Benzenesulfonamide, 2-propyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

146533-54-2

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146533-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146533-54-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,5,3 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 146533-54:
(8*1)+(7*4)+(6*6)+(5*5)+(4*3)+(3*3)+(2*5)+(1*4)=132
132 % 10 = 2
So 146533-54-2 is a valid CAS Registry Number.

146533-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-propylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names 2-propyl-benzenesulfonic acid amide

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:146533-54-2 SDS

146533-54-2Upstream product

146533-54-2Downstream Products

146533-54-2Relevant articles and documents

ARTIFICIAL METALLOENZYMES CONTAINING NOBLE METAL-PORPHYRINS

-

Paragraph 0290; 0293; 0294, (2018/11/21)

The present invention is drawn to artificial metalloenzymes for use in cyclopropanation reactions, amination and C—H insertion.

Chemoselective, enzymatic C-H bond amination catalyzed by a cytochrome P450 containing an Ir(Me)-PIX cofactor

Dydio, Pawel,Key, Hanna M.,Hayashi, Hiroki,Clark, Douglas S.,Hartwig, John F.

, p. 1750 - 1753 (2017/02/15)

Cytochrome P450 enzymes have been engineered to catalyze abiological C-H bond amination reactions, but the yields of these reactions have been limited by low chemoselectivity for the amination of C-H bonds over competing reduction of the azide substrate t

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