67037-01-8

Basic information

• Product Name: (5-PHENYL-TETRAZOL-2-YL)-ACETIC ACID HYDRAZIDE
• Synonyms: ART-CHEM-BB B018648;AKOS B018648;(5-PHENYL-TETRAZOL-2-YL)-ACETIC ACID HYDRAZIDE;2-(5-PHENYL-2H-1,2,3,4-TETRAAZOL-2-YL)ACETOHYDRAZIDE;2-(5-PHENYL-2H-TETRAZOL-2-YL)ACETOHYDRAZIDE;TIMTEC-BB SBB009467;2-(5-phenyl-2H-tetraazol-2-yl)acetohydrazide
• CAS NO: 67037-01-8
• Molecular Formula: C₉H₁₀N₆O
• Molecular Weight: 218.22
• Mol File: 67037-01-8.mol
• Article Data: 8

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.51g/cm³
• Refractive Index: 1.735
• CAS DataBase Reference: (5-PHENYL-TETRAZOL-2-YL)-ACETIC ACID HYDRAZIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (5-PHENYL-TETRAZOL-2-YL)-ACETIC ACID HYDRAZIDE(67037-01-8)
• EPA Substance Registry System: (5-PHENYL-TETRAZOL-2-YL)-ACETIC ACID HYDRAZIDE(67037-01-8)

Safety Data

• Hazardous Substances Data: 67037-01-8(Hazardous Substances Data)

Usage

General 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 commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. (5-PHENYL-TETRAZOL-2-YL)-ACETIC ACID HYDRAZIDE possesses a tetrazole ring, which makes it a potential bioactive molecule with various applications. Its hydrazide group also makes it a valuable intermediate for the synthesis of diverse organic compounds due to its reactivity with other functional groups. Overall, "(5-Phenyl-tetrazol-2-yl)-acetic acid hydrazide" is a versatile chemical with potential applications in the pharmaceutical and agricultural industries.

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)

Upstream product

• 100-47-0 benzonitrile 
• 25828-29-9 (5-phenyltetrazol-2-yl)acetic acid methyl ester 
• 18039-42-4 5-phenyl-2H-1,2,3,4-tetrazole 
• 21743-68-0 5-phenyl-2H-tetrazolylacetic acid 
• 165816-78-4 2-(5-phenyl-2H-tetrazol-2-yl)acetic acid chloride 
• 21054-65-9 5-phenyl-2-tetrazolylacetic acid ethyl ester 

Downstream Products

• 76507-06-7 1-(5-phenyl-2H-tetrazol-2-ylacetyl)-4-(4-tolyl)thiosemicarbazide 
• 127221-40-3 4-nitro-N'-(2-(5-phenyl-2H-tetrazol-2-yl)acetyl)benzohydrazide 
• 127221-42-5 2-chloro-N'-(2-(5-phenyl-2H-tetrazol-2-yl)acetyl)benzohydrazide 
• 1630042-19-1 2-bromo-N'-(2-(5-phenyl-2H-tetrazol-2-yl)acetyl)benzohydrazide 
• 1630042-20-4 2-chloro-5-nitro-N'-(2-(5-phenyl-2H-tetrazol-2-yl)acetyl)benzohydrazide 
• 1630042-21-5 3,5-dimethoxy-N'-(2-(5-phenyl-2H-tetrazol-2-yl)acetyl)benzohydrazide 
• 1630042-22-6 4-bromo-3,5-dimethoxy-N'-(2-(5-phenyl-2H-tetrazol-2-yl)acetyl)benzohydrazide 
• 493003-26-2 N'-(2-(5-phenyl-2H-tetrazol-2-yl)acetyl)furan-2-carbohydrazide 
• 1630042-23-7 2-oxo-N'-(2-(5-phenyl-2H-tetrazol-2-yl)acetyl)-2H-chromene-3-carbohydrazide 
• 1630042-24-8 (E)-3-(4-methoxyphenyl)-N'-(2-(5-phenyl-2H-tetrazol-2-yl)acetyl)acrylohydrazide 
• 1630042-25-9 N'-(2-(5-phenyl-2H-tetrazol-2-yl)acetyl)pivalohydrazide 

Relevant articles and documents

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

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

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

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