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64415-10-7

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64415-10-7 Usage

General Description

N-(O-Chlorobenzyl)hydrazide dihydrochloride is a chemical compound that consists of hydrazide functional group attached to a chlorobenzyl group. It is commonly used in organic synthesis and has been studied for its potential as an antitubercular and antimalarial agent. N-(O-CHLOROBENZYL)HYDRAZIDE DIHYDROCHLORIDE has also been investigated for its potential use in the treatment of various diseases such as cancer and autoimmune disorders. Its dihydrochloride form makes it more stable and soluble, allowing for easier handling and use in various research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 64415-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,1 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64415-10:
(7*6)+(6*4)+(5*4)+(4*1)+(3*5)+(2*1)+(1*0)=107
107 % 10 = 7
So 64415-10-7 is a valid CAS Registry Number.

64415-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Hydrazine, [(2-?chlorophenyl)?methyl]?-?, hydrochloride (1:2)

1.2 Other means of identification

Product number -
Other names -

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:64415-10-7 SDS

64415-10-7Downstream Products

64415-10-7Relevant articles and documents

N-Amino-1,8-Naphthalimide is a Regenerated Protecting Group for Selective Synthesis of Mono-N-Substituted Hydrazines and Hydrazides

Manoj Kumar, Mesram,Venkataramana, Parikibanda,Yadagiri Swamy, Parikibanda,Chityala, Yadaiah

supporting information, p. 17713 - 17721 (2021/11/10)

A new route to synthesis of various mono-N-substituted hydrazines and hydrazides by involving in a new C?N bond formation by using N-amino-1,8-naphthalimide as a regenerated precursor was invented. Aniline and phenylhydrazines are reproduced upon reacting these individually with 1,8-naphthalic anhydride followed by hydrazinolysis. The practicality and simplicity of this C?N dihalo alkanes; developed a synthon for bond formation protocol was exemplified to various hydrazines and hydrazides. N-amino-1,8-naphthalimide is suitable synthon for transformation for selective formation of mono-substituted hydrazine and hydrazide derivatives. Those are selective mono-amidation of hydrazine with acid halides; mono-N-substituted hydrazones from aldehydes; synthesis of N-aminoazacycloalkanes from acetohydrazide scaffold and inserted to hydroxy derivatives; distinct synthesis of N,N-dibenzylhydrazines and N-benzylhydrazines from benzyl halides; synthesis of N-amino-amino acids from α-halo esters. Ecofriendly reagent N-amino-1,8-naphthalimide was regenerated with good yields by the hydrazinolysis in all procedures.

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