1-(1H-Benzimidazol-2-yl)-3-(4-chlorophenyl)-2-propen-1-one

Base Information

Chemical Name:1-(1H-Benzimidazol-2-yl)-3-(4-chlorophenyl)-2-propen-1-one
CAS No.:36998-77-3
Molecular Formula:C16H11 Cl N2 O
Molecular Weight:282.729
Hs Code.:2933990090
NSC Number:716333
Nikkaji Number:J2.793.200B
Wikidata:Q76309062
ChEMBL ID:CHEMBL1996220
Mol file:36998-77-3.mol

Synonyms:1-(1H-Benzimidazol-2-yl)-3-(4-chlorophenyl)-2-propen-1-one;36998-77-3;2-Propen-1-one, 1-(1H-benzimidazol-2-yl)-3-(4-chlorophenyl)-;NSC716333;CHEMBL1996220;AKOS002679953;NSC-716333;LS-123810;(2E)-1-(1H-Benzoimidazole-2-yl)-3-(4-chlorophenyl)-2-propene-1-one

Suppliers and Price of 1-(1H-Benzimidazol-2-yl)-3-(4-chlorophenyl)-2-propen-1-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
2-PROPEN-1-ONE, 1-(1H-BENZIMIDAZOL-2-YL)-3-(4-CHLOROPHENYL)- 95.00%
5MG
$ 497.65

Total 3 raw suppliers

Chemical Property of 1-(1H-Benzimidazol-2-yl)-3-(4-chlorophenyl)-2-propen-1-one

Chemical Property:

Vapor Pressure:6.76E-11mmHg at 25°C
Boiling Point:519.5°Cat760mmHg
Flash Point:268°C
PSA：45.75000
Density:1.362g/cm³
LogP:4.11240
XLogP3:4.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:282.0559907
Heavy Atom Count:20
Complexity:377

Purity/Quality:

99% ^*data from raw suppliers

2-PROPEN-1-ONE, 1-(1H-BENZIMIDAZOL-2-YL)-3-(4-CHLOROPHENYL)- 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)NC(=N2)C(=O)C=CC3=CC=C(C=C3)Cl
Isomeric SMILES:C1=CC=C2C(=C1)NC(=N2)C(=O)/C=C/C3=CC=C(C=C3)Cl

Technology Process of 1-(1H-Benzimidazol-2-yl)-3-(4-chlorophenyl)-2-propen-1-one

There total 6 articles about 1-(1H-Benzimidazol-2-yl)-3-(4-chlorophenyl)-2-propen-1-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%