136689-94-6

Basic information

• Product Name: 3-(1H-TETRAZOL-5-YL)BENZALDEHYDE
• Synonyms: 3-(1H-TETRAZOL-5-YL)BENZALDEHYDE;3-(2H-Tetrazol-5-yl)benzaldehyde;3-(2H-1,2,3,4-tetrazol-5-yl)benzaldehyde
• CAS NO: 136689-94-6
• Molecular Formula: C₈H₆N₄O
• Molecular Weight: 174.15944
• Mol File: 136689-94-6.mol
• Article Data: 12

Chemical Properties

• Melting Point: 196-198 °C
• Boiling Point: 416.0±47.0 °C(Predicted)
• Appearance: /
• Density: 1.400±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 3.99±0.10(Predicted)
• CAS DataBase Reference: 3-(1H-TETRAZOL-5-YL)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1H-TETRAZOL-5-YL)BENZALDEHYDE(136689-94-6)
• EPA Substance Registry System: 3-(1H-TETRAZOL-5-YL)BENZALDEHYDE(136689-94-6)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 136689-94-6(Hazardous Substances Data)

Usage

General Description

3-(1H-tetrazol-5-yl)benzaldehyde is a compound consisting of a benzene ring with a tetrazol-5-yl group and an aldehyde functional group attached to it. This chemical is commonly used as a building block in the synthesis of pharmaceutical and agrochemical compounds, and as a chemical intermediate in organic synthesis. It is also known for its potential biological activity and has been studied for its potential use in the pharmaceutical industry. Additionally, it has been investigated for its potential use in the development of new materials and as a reagent in organic chemistry reactions.

Upstream product

• 24964-64-5 3-Cyanobenzaldehyde 
• 1877-72-1 3-Cyanobenzoic acid 
• 3132-99-8 m-bromobenzoic aldehyde 
• 945981-95-3 3-cyanobenzaldehyde diethyl acetal 
• 945981-72-6 5-(3-diethoxymethylphenyl)-1-triphenylmethyl-1H-tetrazole 
• 179057-20-6 [3-(1H-tetrazol-5-yl)phenyl]methanol 
• 148345-63-5 methyl 3-(1H-tetrazol-5-yl)benzoate 
• 1711-11-1 3-cyanobenzoyl chloride 
• 13531-48-1 methyl 3-cyanobenzoate 

Downstream Products

• 179056-01-0 3-(2-methyl-tetrazol-5-yl)-benzaldehyde 

Relevant articles and documents

Zinc hydroxyapatite - Catalyzed efficient synthesis of 5-substituted 1H-tetrazoles

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Facile, highly efficient and novel method for synthesis of 5-substituted 1H-tetrazoles catalysed by copper(I) chloride

The present study on tetrazole compounds, which have a wide area of application, proposes a new, simple and highly effective method. A series of 5-substituted 1H-tetrazoles were synthesised in DMF via the [3 + 2] cycloaddition reaction, in which different

Design, synthesis and evaluation of 1,3,6-trisubstituted-4-oxo-1,4-dihydroquinoline-2-carboxylic acid derivatives as ETA receptor selective antagonists using FRET assay

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Identification of a New Class of Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitors Followed by a Structure-Activity Relationship Study

Screening of a small compound library at the three excitatory amino acid transporter subtypes 1-3 (EAAT1-3) resulted in the identification of compound (Z)-4-chloro-3-(5-((3-(2-ethoxy-2-oxoethyl)-2,4-dioxothiazolidin-5-ylidene)methyl)furan-2-yl)benzoic aci