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21150-15-2

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21150-15-2 Usage

Type of compound

Organic compound

Functional group

Hydrazine functional group

Additional groups

Two benzoyl groups

Usage

Reagent in organic synthesis

Application

Building block in the production of pharmaceuticals and agrochemicals

Potential use

Treatment of cancer and other diseases

Known properties

Carcinogenic and mutagenic

Safety precautions

Proper handling and safety measures should be taken to minimize risk of exposure

Check Digit Verification of cas no

The CAS Registry Mumber 21150-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,1,5 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21150-15:
(7*2)+(6*1)+(5*1)+(4*5)+(3*0)+(2*1)+(1*5)=52
52 % 10 = 2
So 21150-15-2 is a valid CAS Registry Number.

21150-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-benzoyl-N'-methylbenzohydrazide

1.2 Other means of identification

Product number -
Other names 1,2-Dibenzoyl-1-methylhydrazine

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:21150-15-2 SDS

21150-15-2Downstream Products

21150-15-2Relevant articles and documents

Evidence of an nN(amide) → π*ArInteraction in N-Alkyl- N, N′-diacylhydrazines

Deka, Jugal Kishore Rai,Sahariah, Biswajit,Sakpal, Sushil S.,Bar, Arun Kumar,Bagchi, Sayan,Sarma, Bani Kanta

supporting information, p. 7003 - 7007 (2021/05/26)

1,2-Dibenzoyl-1-tert-butylhydrazine (RH-5849) and related N-alkyl-N,N′-diacylhydrazines are environmentally benign insect growth regulators. Herein, we show that an unusual nN(amide) → π*Ar interaction mediated by a hydrazide amide nitrogen atom plays a crucial role in stabilizing their biologically active trans-cis (t-c) rotameric conformations. We provide NMR and IR spectroscopic evidence for the presence of these interactions, which is also supported by X-ray crystallographic and computational studies.

Synthesis of 3-methyl-[1,2,4]-triazepino[6,5,4-jk]carbazol-4(3H)one

Peet,Sunder

, p. 1147 - 1150 (2007/10/05)

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