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1073-62-7

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1073-62-7 Usage

Description

BENZYLHYDRAZINE MONOHYDROCHLORIDE is an arylhydrazine derivative characterized by its pale yellow solid appearance and mutagenic properties. It is a chemical compound that holds potential in various applications due to its unique chemical structure and properties.

Uses

Used in Pharmaceutical Industry:
BENZYLHYDRAZINE MONOHYDROCHLORIDE is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its mutagenic properties make it a valuable component in the development of drugs that target specific biological pathways.
Used in Chemical Research:
In the field of chemical research, BENZYLHYDRAZINE MONOHYDROCHLORIDE serves as a key substance for studying the properties and reactions of arylhydrazine derivatives. This aids in understanding their behavior and potential applications in different chemical processes.
Used in Organic Synthesis:
BENZYLHYDRAZINE MONOHYDROCHLORIDE is utilized as a reagent in organic synthesis, particularly for the preparation of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, contributing to the synthesis of complex organic molecules.
Used in Analytical Chemistry:
In analytical chemistry, BENZYLHYDRAZINE MONOHYDROCHLORIDE can be employed as a reference compound for the development and calibration of analytical methods. Its distinct properties make it suitable for use in the validation of techniques and instruments in this field.

Safety Profile

Poison by ingestion andintraperitoneal route. When heated to decomposition itemits very toxic fumes of NOx and Cl-.

Check Digit Verification of cas no

The CAS Registry Mumber 1073-62-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1073-62:
(6*1)+(5*0)+(4*7)+(3*3)+(2*6)+(1*2)=57
57 % 10 = 7
So 1073-62-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2/c8-9-6-7-4-2-1-3-5-7/h1-5H,6,9H2,8H3/q+2

1073-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzylhydrazine Monohydrochloride

1.2 Other means of identification

Product number -
Other names Benzylhydrazine hydrochloride

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:1073-62-7 SDS

1073-62-7Relevant articles and documents

Decarboxylative hydrazination of unactivated carboxylic acids by cerium photocatalysis

Yatham, Veera Reddy,Bellotti, Peter,K?nig, Burkhard

, p. 3489 - 3492 (2019)

We report the cerium photocatalyzed radical decarboxylative hydrazination of carboxylic acids with di-tert-butylazodicarboxylate (DBAD). The operationally simple protocol provides rapid access to synthetically useful hydrazine derivatives and overcomes current scope limitations in the photoredox-catalyzed decarboxylation of carboxylic acids.

N-tert-butoxycarbonylaminophthalimide, a versatile reagent for the conversion of alcohols into alkylated tert-butylcarbazates or hydrazines via the Mitsunobu protocol

Brosse, Nicolas,Pinto, Maria-Fatima,Jamart-Grégoire, Brigitte

, p. 205 - 207 (2007/10/03)

An efficient two-step method has been developed for the conversion of alcohols to substituted hydrazines. The use of N-tert- butoxycarbonylaminophthalimide as an acid partner in Mitsunobu reactions with a variety of alcohols permits the synthesis of the corresponding monoalkylated tert-butylcarbazates and hydrazines.

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