2-[(E)-prop-1-enyl]-1H-benzimidazole

Base Information

Chemical Name:2-[(E)-prop-1-enyl]-1H-benzimidazole
CAS No.:7464-22-4
Molecular Formula:C₁₀H₁₀N₂
Molecular Weight:158.203
Hs Code.:
European Community (EC) Number:659-597-7
NSC Number:403382
DSSTox Substance ID:DTXSID40419677
Nikkaji Number:J3.012.391C
Wikidata:Q76306108
Mol file:7464-22-4.mol

Synonyms:2-[(E)-prop-1-enyl]-1H-benzimidazole;105259-40-3;NSC403382;1H-Benzimidazole,2-(1-propenyl)-,(E)-(9CI);7464-22-4;2-(1-Propenyl)-1H-benzoimidazole;2-(Prop-1-en-1-yl)-1H-benzo[d]imidazole;(E)-2-(Prop-1-en-1-yl)-1H-benzo[d]imidazole;DTXSID40419677;AKOS024340558;NSC-403382;2-[(1E)-1-propenyl]-1H-benzimidazole

Suppliers and Price of 2-[(E)-prop-1-enyl]-1H-benzimidazole

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

AccelPharmtech
2-(1-propen-1-yl)-1H-Benzimidazole 97.00%
25G
$ 3120.00

AccelPharmtech
2-(1-propen-1-yl)-1H-Benzimidazole 97.00%
5G
$ 1700.00

AccelPharmtech
2-(1-propen-1-yl)-1H-Benzimidazole 97.00%
1G
$ 1530.00

Total 6 raw suppliers

Chemical Property of 2-[(E)-prop-1-enyl]-1H-benzimidazole

Chemical Property:

Vapor Pressure:0.000106mmHg at 25°C
Boiling Point:337.3°Cat760mmHg
Flash Point:171.8°C
PSA：28.68000
Density:1.162g/cm³
LogP:2.59600
XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:158.084398327
Heavy Atom Count:12
Complexity:177

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

2-(1-propen-1-yl)-1H-Benzimidazole 97.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC=CC1=NC2=CC=CC=C2N1
Isomeric SMILES:C/C=C/C1=NC2=CC=CC=C2N1

Technology Process of 2-[(E)-prop-1-enyl]-1H-benzimidazole

There total 1 articles about 2-[(E)-prop-1-enyl]-1H-benzimidazole 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: 94.0%

: 6117-91-5,542-72-3
(E/Z)-2-buten-1-ol

: 95-54-5
1,2-diamino-benzene

: 7464-22-4
C₁₀H₁₀N₂

Guidance literature:: With dimethyl sulfoxide; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; In ethyl acetate; at 0 - 25 ℃; for 2.5h; chemoselective reaction; Inert atmosphere;
DOI:10.1016/j.tetlet.2011.08.037