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2-Phenylbenzimidazole, 98%|254628|716-79-0

2-Phenylbenzimidazole, 98%

Cat. No JK254628_5_G
J&K Chemical

Product Information

Product Name
2-Phenylbenzimidazole, 98%
Brand Name
J&K
Product Number
254628
CAS
716-79-0
Molecular Formula
C13H10N2
Molecular Weight
194.23
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
12855
IUPAC Name
2-phenyl-1H-benzimidazole
InChI Key
DWYHDSLIWMUSOO-UHFFFAOYSA-N
SMILES
C1=CC=C(C=C1)C2=NC3=CC=CC=C3N2

Properties

Melting Point
293-296

Safety Information

Signal Word
Warning
Hazard Statement
H302
H315
H319
H335
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P319
P405
P301+P317
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Design and application of silica-coated magnetic Fe3O4 nanoparticles immobilized with bis(serinyl)triazine–copper complex as an efficient catalyst for the green synthesis of benzimidazoles
Publication Name: Research on Chemical Intermediates
Publication Date: 2026-01-13
DOI: 10.1007/s11164-025-05901-0

Catalyst-Assisted Synthesis of Benzimidazole Derivatives: Recent Advances and Mechanistic Insights
Publication Name: Topics in current chemistry (Cham)
Publication Date: 2026-01-03
DOI: 10.1007/s41061-025-00535-7

Synthesis of imidazo[2,1-a]isoquinolin-5-ones via C–H imidoylmethylation/oxidation/cyclization cascade of 2-arylbenzimidazoles with CF3-imidoyl sulfoxonium ylides by Rh(III)/Cu(II) relay catalysis
Publication Name: Molecular Diversity
Publication Date: 2025-12-19
DOI: 10.1007/s11030-025-11428-8

Study on the metal interface adsorption behavior of nitrogen heterocyclic corrosion inhibitors
Publication Name: Applied Physics A
Publication Date: 2025-10-31
DOI: 10.1007/s00339-025-09043-3

Halogenation of 2H-thiopyrans containing 3-positioned electron-withdrawing substituents
Publication Name: Russian Chemical Bulletin
Publication Date: 2025-09
DOI: 10.1007/s11172-025-4767-3

2-Phenylbenzimidazole, 98%

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