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24642-84-0

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24642-84-0 Usage

Structure

Hydrazine derivative with a tert-butyl group and a phenyl group attached to the nitrogen atom

Usage

Commonly used as a reagent in organic synthesis

Applications

Preparation of pharmaceuticals and agrochemicals

Role

Useful intermediate in the production of various chemical compounds

Safety precautions

Potentially hazardous if not properly handled and used in a controlled environment

Check Digit Verification of cas no

The CAS Registry Mumber 24642-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,4 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24642-84:
(7*2)+(6*4)+(5*6)+(4*4)+(3*2)+(2*8)+(1*4)=110
110 % 10 = 0
So 24642-84-0 is a valid CAS Registry Number.

24642-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-tert-butyl-N-phenylnitrous amide

1.2 Other means of identification

Product number -
Other names 1-tert-butyl-2-oxo-1-phenylhydrazine

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:24642-84-0 SDS

24642-84-0Relevant articles and documents

Rhodium(III)-catalyzed N-nitroso-directed C-H olefination of arenes. High-yield, versatile coupling under mild conditions

Liu, Baoqing,Fan, Yang,Gao, Yang,Sun, Chao,Xu, Cheng,Zhu, Jin

supporting information, p. 468 - 473 (2013/02/23)

N-Nitroso compounds are a versatile class of organic structures that allow expedient access to a diversity of synthetically useful architectures through demonstrated reactivities. We report herein the development of a Rh(III)-catalyzed N-nitroso-directed

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