[1-(1-phenylethyl)-1H-benzimidazol-2-yl]methanol

Base Information

Chemical Name:[1-(1-phenylethyl)-1H-benzimidazol-2-yl]methanol
CAS No.:380551-61-1
Molecular Formula:C₁₆H₁₆N₂O
Molecular Weight:252.316
Hs Code.:
DSSTox Substance ID:DTXSID701333502
ChEMBL ID:CHEMBL1532609
Mol file:380551-61-1.mol

Synonyms:380551-61-1;[1-(1-phenylethyl)-1H-benzimidazol-2-yl]methanol;[1-(1-phenylethyl)benzimidazol-2-yl]methanol;(1-(1-phenylethyl)-1H-benzo[d]imidazol-2-yl)methanol;[1-(1-phenylethyl)-1H-1,3-benzodiazol-2-yl]methanol;Oprea1_541559;Oprea1_607754;MLS001209813;[1-(1-Phenyl-ethyl)-1H-benzoimidazol-2-yl]-methanol;IFLab1_004052;CHEMBL1532609;SCHEMBL16756383;DTXSID701333502;HMS1423I04;HMS2821G03;MFCD02630597;STK738030;AKOS000272072;AKOS016040818;BS-33476;SMR000518657;CS-0208434;AF-399/15335523;A1-09357;Z57299977;[1-(1-phenylethyl)-1H-1,3-benzimidazol-2-yl]methanol;F0853-0189

Suppliers and Price of [1-(1-phenylethyl)-1H-benzimidazol-2-yl]methanol

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

Matrix Scientific
(1-(1-Phenylethyl)-1H-benzo[d]imidazol-2-yl)methanol 95%
5g
$ 1650.00

A1 Biochem Labs
(1-(1-Phenylethyl)-1H-benzo[d]imidazol-2-yl)methanol 95%
1 g
$ 450.00

Total 2 raw suppliers

Chemical Property of [1-(1-phenylethyl)-1H-benzimidazol-2-yl]methanol

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:252.126263138
Heavy Atom Count:19
Complexity:291

Purity/Quality:

99% ^*data from raw suppliers

(1-(1-Phenylethyl)-1H-benzo[d]imidazol-2-yl)methanol 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C1=CC=CC=C1)N2C3=CC=CC=C3N=C2CO

Technology Process of [1-(1-phenylethyl)-1H-benzimidazol-2-yl]methanol

There total 4 articles about [1-(1-phenylethyl)-1H-benzimidazol-2-yl]methanol 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: 63.0%

: 1039987-39-7
N¹-(1-phenylethyl)benzene-1,2-diamine

: 79-14-1
glycolic Acid

: 380551-61-1
[1-(1-phenylethyl)-1H-benzimidazol-2-yl]methanol

Guidance literature:: In methanol; at 80 ℃; for 18h;

Reference yield:

: 1493-27-2,127723-77-7
ortho-nitrofluorobenzene

: 380551-61-1
[1-(1-phenylethyl)-1H-benzimidazol-2-yl]methanol

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / ethanol / 6 h / 0 - 80 °C

2: zinc; ammonium formate / methanol / 5 h / 0 - 20 °C

3: methanol / 18 h / 80 °C

With ammonium formate; triethylamine; zinc; In methanol; ethanol;

Reference yield:

: 618-36-0
rac-methylbenzylamine

: 380551-61-1
[1-(1-phenylethyl)-1H-benzimidazol-2-yl]methanol

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / ethanol / 6 h / 0 - 80 °C

2: zinc; ammonium formate / methanol / 5 h / 0 - 20 °C

3: methanol / 18 h / 80 °C

With ammonium formate; triethylamine; zinc; In methanol; ethanol;