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67037-01-8

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67037-01-8 Usage

Description

(5-PHENYL-TETRAZOL-2-YL)-ACETIC ACID HYDRAZIDE is a chemical compound that belongs to the class of hydrazides, which are derivatives of hydrazine. It is characterized by the presence of a tetrazole ring and a hydrazide group, making it a potential bioactive molecule with various applications. This versatile chemical is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals, and its reactivity with other functional groups makes it a valuable intermediate for the synthesis of diverse organic compounds.

Uses

Used in Pharmaceutical Industry:
(5-PHENYL-TETRAZOL-2-YL)-ACETIC ACID HYDRAZIDE is used as a building block for the synthesis of various pharmaceuticals due to its potential bioactivity and reactivity with other functional groups. Its tetrazole ring and hydrazide group contribute to the development of new drugs with improved properties and therapeutic effects.
Used in Agrochemical Industry:
(5-PHENYL-TETRAZOL-2-YL)-ACETIC ACID HYDRAZIDE is used as a key intermediate in the synthesis of agrochemicals, particularly in the development of new pesticides and other agricultural chemicals. Its versatility and reactivity allow for the creation of novel compounds with enhanced efficacy and selectivity in controlling pests and diseases in the agricultural sector.
Used in Organic Synthesis:
(5-PHENYL-TETRAZOL-2-YL)-ACETIC ACID HYDRAZIDE is used as a valuable intermediate for the synthesis of diverse organic compounds. Its reactivity with other functional groups enables the development of new molecules with various applications, such as in the fields of materials science, chemical research, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 67037-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,3 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67037-01:
(7*6)+(6*7)+(5*0)+(4*3)+(3*7)+(2*0)+(1*1)=118
118 % 10 = 8
So 67037-01-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N6O/c10-11-8(16)6-15-13-9(12-14-15)7-4-2-1-3-5-7/h1-5H,6,10H2,(H,11,16)

67037-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-phenyltetrazol-2-yl)acetohydrazide

1.2 Other means of identification

Product number -
Other names 5-phenyl-2-tetrazolylacetic acid hydrazide

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:67037-01-8 SDS

67037-01-8Relevant articles and documents

Novel ((phenyltetrazolyl)methyl)oxadiazole derivatives and use thereof

-

, (2017/01/17)

The present invention relates to a compound represented by chemical formula I or a pharmaceutically acceptable salt thereof, and to a pharmaceutical composition and a functional health food comprising the compound or the pharmaceutically acceptable salt thereof as an active component for preventing or treating bone diseases. More particularly, the composition of the present invention has an effect of suppressing differentiation and activation of osteoclasts and can suppress bone diseases caused by bone loss, thereby being useful as a pharmaceutical composition for preventing or treating the diseases.COPYRIGHT KIPO 2016

Novel N-acyl/aroyl-2-(5-phenyl-2H-tetrazol-2-yl)acetohydrazides: Synthesis and characterization

Saeed, Aamer,Hussain, Majid,Qasim, Muhammad

, p. 436 - 442 (2014/06/09)

A number of novel N -acyl/aroyl-2-(5-phenyl-2H-tetrazol-2-yl) acetohydrazides (4a-j) of biological interest were efficiently synthesized by treating 2-(5-phenyl-2H-tetrazole-2-yl)acetohydrazide (3) with a variety of aroyl/heterocyclyl or alkanoyl chlorides. FTIR, 1H NMR, 13C NMR, GC-MS, and elemental analyses data confirmed the structures assigned to the newly synthesized compounds. TUeBITAK.

Aminolysis of 5-phenyl-2-tetrazolylacetic acid ethyl ester

Putis,Zubarev,Poplavskii,Ostrovskii

, p. 698 - 701 (2007/10/03)

It was shown using 5-phenyl-2-tetrazolylacetic acid ethyl ester as an example that aminolysis is a competitive method of synthesizing primary amides. The efficiency of aminolysis by primary amines is linked to the basicity of the initial amine. Highly bas

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