90514-72-0

Basic information

• Product Name: 4-(1H-1,3-BENZIMIDAZOL-1-YL)BENZENECARBALDEHYDE
• Synonyms: ASINEX-REAG BAS 10156674;4-BENZOIMIDAZOL-1-YL-BENZALDEHYDE;4-(1H-1,3-BENZIMIDAZOL-1-YL)BENZENECARBALDEHYDE;4-(benzimidazol-1-yl)benzaldehyde
• CAS NO: 90514-72-0
• Molecular Formula: C₁₄H₁₀N₂O
• Molecular Weight: 222.24
• Mol File: 90514-72-0.mol
• Article Data: 18

Chemical Properties

• Melting Point: 98-100°C
• Boiling Point: 428.5 °C at 760 mmHg
• Flash Point: 212.9 °C
• Appearance: /
• Density: 1.19 g/cm³
• PKA: 3.91±0.10(Predicted)
• CAS DataBase Reference: 4-(1H-1,3-BENZIMIDAZOL-1-YL)BENZENECARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1H-1,3-BENZIMIDAZOL-1-YL)BENZENECARBALDEHYDE(90514-72-0)
• EPA Substance Registry System: 4-(1H-1,3-BENZIMIDAZOL-1-YL)BENZENECARBALDEHYDE(90514-72-0)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 90514-72-0(Hazardous Substances Data)

Usage

General Description

4-(1H-1,3-benzimidazol-1-yl)benzenecarbaldehyde is a chemical compound with the molecular formula C14H10N2O. It is a benzaldehyde derivative that contains a benzimidazole ring. 4-(1H-1,3-BENZIMIDAZOL-1-YL)BENZENECARBALDEHYDE has potential biological activities and is being studied for its pharmacological properties. It is often used as a building block in organic synthesis and medicinal chemistry. Additionally, it is a part of the chemical structure of some pharmaceutical drugs and is being researched for its potential therapeutic applications.

Upstream product

• 51-17-2 benzoimidazole 
• 459-57-4 4-fluorobenzaldehyde 
• 104-88-1 4-chlorobenzaldehyde 
• 1122-91-4 4-bromo-benzaldehyde 
• 87199-17-5 4-formylphenylboronic acid, 

Downstream Products

• 90514-75-3 1-[4-((E)-2-Nitro-propenyl)-phenyl]-1H-benzoimidazole 
• 117607-04-2 6-[(E)-2-(4-Benzoimidazol-1-yl-phenyl)-vinyl]-5-methyl-4,5-dihydro-2H-pyridazin-3-one 
• 108122-61-8 1-(4-Benzoimidazol-1-yl-phenyl)-propan-2-one 
• 90514-84-4 5-(4-Benzoimidazol-1-yl-phenyl)-6-methyl-2-oxo-1,2-dihydro-pyridine-3-carbonitrile 
• 666850-93-7 (4aS,8aR)-2-[1-(4-benzimidazol-1-yl-benzyl)-piperidin-4-yl]-4-(3,4-dimethoxy-phenyl)-4a,5,8,8a-tetrahydro-2H-phthalazin-1-one hydrochloride 
• 1392592-91-4 4-(4-(1H-benzo[d]imidazol-1-yl)phenyl)-6-(2,4-dichlorophenyl)pyrimidin-2-amine 
• 1392592-89-0 4-(4-(1H-benzo[d]imidazol-1-yl)phenyl)-6-(4 fluorophenyl)pyrimidin-2-amine 
• 1392592-92-5 4-(4-(1H-benzo[d]imidazol-1-yl) phenyl)-6-(4-bromophenyl)pyrimidin-2-amine 
• 1392592-90-3 4-(4-(1H-benzo[d]imidazol-1-yl)phenyl)-6-(4-chlorophenyl)pyrimidin-2-amine 
• 1392592-93-6 4-(4-(1H-benzo[d]imidazol-1-yl) phenyl)-6-(4-methoxyphenyl)pyrimidin-2-amine 
• 220495-52-3 4-(benzimidazole-1-yl)benzoic acid 

Relevant articles and documents

Synthesis and antimicrobial activity of novel 2-[4-(1H-benzimidazol-1-yl) phenyl]-1H-benzimidazoles

A new class of 2-[4-(1H-benzimidazol-1-yl)phenyl]-1H-benzimidazoles (13-22) were synthesized via cyclocondensation reaction of the substituted 1,2-phenylenediamines (1, 4-12) and 1-(4-formylpheny)-1H-benzimidazole (3). The synthesized compounds were evalu

Cu(OAc)2-porphyrins as an efficient catalytic system for base-free, nature mimicking Chan–Lam coupling in water

The use of porphyrins as ligands in organic synthesis reveals the natural process, because these are the constituent motifs of catalysts in many bio-organic reactions. This article presents the synthesis of two N-pincer tetradentate porphyrins; tetrasodium meso-tetra(p-sulfonatophenyl)phorphyrin (H2TSTpSPP) and meso-tetra(m-carboxyphenyl)porphyrin (H2TmCPP), and study on their aptness for Cu-catalyzed C–N coupling reactions of arylboronic acids and amines (Chan–Lam coupling reaction) in water under external base free conditions. The porphyrins and Chan–Lam coupling products were well characterized by their spectral analysis. The high product yields, application of nature-inspired conditions, large extent of substrates, ease of making and handling the ligands, avoidance of base, and use of water as reaction media are the attractive attributes of this finding.

Benzimidazole benzaldehyde fluorescein hydrazide Schiff base and preparation method thereof

The invention belongs to the field of fluorescent probes, and particularly relates to benzimidazole benzaldehyde fluorescein hydrazide Schiff base and a preparation method thereof. The probe is a turn-on type fluorescent probe, the probe utilizes a photoi

PROTEIN-PROTEIN INTERACTION STABILIZERS

Provided herein, inter alia, are stabilizers of protein-protein interactions and methods of identifying and using the same.