82544-82-9

Basic information

• Product Name: Methyl 4-(2H-1,2,3,4-tetrazol-5-yl)benzoate
• Synonyms: Methyl 4-(2H-1,2,3,4-tetrazol-5-yl)benzoate;Methyl 4-(1H-tetrazol-5-yl)benzoate
• CAS NO: 82544-82-9
• Molecular Formula: C₉H₈N₄O₂
• Molecular Weight: 204.18542
• Mol File: 82544-82-9.mol
• Article Data: 22

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Methyl 4-(2H-1,2,3,4-tetrazol-5-yl)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 4-(2H-1,2,3,4-tetrazol-5-yl)benzoate(82544-82-9)
• EPA Substance Registry System: Methyl 4-(2H-1,2,3,4-tetrazol-5-yl)benzoate(82544-82-9)

Safety Data

• Hazardous Substances Data: 82544-82-9(Hazardous Substances Data)

Upstream product

• 1129-35-7 4-cyanobenzoic acid methyl ester 
• 619-65-8 4-cyanobenzoic Acid 
• 67-56-1 methanol 
• 34114-12-0 4-(1H-tetrazol-5-yl)benzoic acid 
• 168699-41-0 methyl 4-[(1E)-(hydroxyimino)methyl]benzoate 
• 53148-13-3 4-(hydroxyiminomethyl)benzoic acid methyl ester 
• 4648-54-8 trimethylsilylazide 
• 99768-12-4 4-methoxycarbonylphenylboronic acid 
• 1571-08-0 methyl 4-formylbenzoate 

Downstream Products

• 85292-39-3 methyl 4-(5-phenyl-1,3,4-oxadiazol-2-yl)benzoate 
• 73670-64-1 2-(4-pentenyl)-5-tetrazole 
• 82544-86-3 3-pyrrolidino<1,2-b>-2-pyrazoline 
• 100964-94-1 4-[5-(4-nitro-phenyl)-[1,3,4]oxadiazol-2-yl]-benzoic acid 
• 85292-45-1 4-(5-phenyl-1,3,4-oxadiazol-2-yl)benzoic acid 
• 34114-12-0 4-(1H-tetrazol-5-yl)benzoic acid 
• 1268102-28-8 fac-[Re(1,10-phenanthroline)(CO)3(methyl 4-(tetrazolate-5-yl)benzoate)] 
• 1268102-26-6 fac-[Re(2,2'-bipyridine)(CO)3(methyl 4-(tetrazolate-5-yl)benzoate)] 
• 34114-12-0 4-(2H-1,2,3,4-tetrazol-5-yl)benzoic acid 
• 201050-72-8 methyl 4-(5-methyl-1,3,4-oxadiazol-2-yl)benzoate 

Relevant articles and documents

Design and Synthesis of a BODIPY-Tetrazole Based “Off-On” in-Cell Fluorescence Reporter of Hydrogen Peroxide

BODIPY-linked bithiophene-tetrazoles were designed and synthesized for bioorthogonal photoclick reactions in vitro and in vivo. The reactivity of these tetrazoles toward dimethyl fumarate was found to depend on the BODIPY attachment site, with the meta-linked BODIPY–tetrazole being the most reactive. The resulting pyrazoline cycloadduct showed drastically reduced BODIPY fluorescence. However, BODIPY fluorescence recovered after treatment with hydrogen peroxide. This turn-on effect was attributed to conversion from the pyrazoline to a pyrazole. Finally, we showed that this unique BODIPY–tetrazole off–on fluorescence probe can be used to detect hydrogen peroxide inside HeLa cells.

One-Pot Suzuki-Hydrogenolysis Protocol for the Modular Synthesis of 2,5-Diaryltetrazoles

2,5-Diaryltetrazoles are a diverse range of compounds of considerable interest within the field of photochemistry as a valuable precursor of the nitrile imine 1,3-dipole. Current literature approaches toward this heterocycle remain unsuitable for the prac

HETEROCYCLIC COMPOUNDS AS FUNGICIDES

The present invention relates to novel heterocyclic compound of Formula (I), (I) wherein, Het, L1, A, L2 and R12 are as defined in the detailed description, for use as fungicides.