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1-BENZYL-1-(4-BROMOBENZYL)HYDRAZINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111515-65-2

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111515-65-2 Usage

Type of compound

Hydrazine derivative

Structural features

Contains both benzyl and bromobenzyl groups

Applications

a. Organic synthesis
b. Pharmaceutical research
c. Building block for the synthesis of biologically active molecules
d. Potential use in the development of new drugs or therapeutic agents

Safety precautions

a. Handle with caution due to potential hazards
b. Use only by trained professionals
c. Follow appropriate safety protocols

Check Digit Verification of cas no

The CAS Registry Mumber 111515-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,5,1 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 111515-65:
(8*1)+(7*1)+(6*1)+(5*5)+(4*1)+(3*5)+(2*6)+(1*5)=82
82 % 10 = 2
So 111515-65-2 is a valid CAS Registry Number.

111515-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-1-[(4-bromophenyl)methyl]hydrazine

1.2 Other means of identification

Product number -
Other names 1-benzyl-1-(4-bromobenzyl)hydrazine

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:111515-65-2 SDS

111515-65-2Relevant academic research and scientific papers

NITRENES. SYNTHESIS OF UNSYMMETRICAL BIBENZYLS

Savin, V. I.

, p. 35 - 41 (2007/10/02)

A method was developed for the synthesis of unsymmetrical bibenzyls by thermolysis of the potassium salts of methanesulfonohydrazides in dimethyl sulfoxide in the presence of 1-pentanethiol.The yields of the unsymmetrical bibenzyls and their derivatives c

N-NITRENES. II. INVESTIGATION OF THE MECHANISM OF DISSOCIATION OF DIBENZYLAMINONITRENE BY CHEMICALLY INDUCED POLARIZATION OF 1H NUCLEI. THE SPIN STATE OF DIBENZYLAMINONITRENE

Savin, V. I.

, p. 15 - 25 (2007/10/02)

The mechanism of the dissociation of dibenzylaminonitrene and p-bromodibenzylaminonitrene into molecular nitrogen and hydrocarbon products was studied.Dibenzylaminonitrene forms dibenzyl and o- and p-benzyltoluenes.In the presence of thiophenol significant amounts of toluene are formed.During dissociation p-bromodibenzylaminonitrene gives a mixture of symmetrical and unsymmetrical dibenzyls.In the presence of octanethiol only unsymmetrical p-bromodibenzyl is formed.The dissociation of dibenzylaminonitrene takes place by synchronous cleavage of the two C-N bonds and the formation of a pair of benzyl radicals.Dibenzylaminonitrene dissociates from the singlet electronic state.

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