[1-(2-fluorophenyl)-1H-pyrrol-2-yl]methanol

Base Information

Chemical Name:[1-(2-fluorophenyl)-1H-pyrrol-2-yl]methanol
CAS No.:132407-66-0
Molecular Formula:C11H10FNO
Molecular Weight:191.2016032
Hs Code.:2933998090
European Community (EC) Number:696-607-9
DSSTox Substance ID:DTXSID30572886
Nikkaji Number:J1.103.715A
Wikidata:Q82461390

Synonyms:[1-(2-fluorophenyl)-1H-pyrrol-2-yl]methanol;132407-66-0;(1-(2-Fluorophenyl)-1H-pyrrol-2-yl)methanol;[1-(2-fluorophenyl)pyrrol-2-yl]methanol;DTXSID30572886;MFCD09754615;AKOS006327550;KG-0701;SB62941;CS-0337853;G54815;EN300-8586146

Suppliers and Price of [1-(2-fluorophenyl)-1H-pyrrol-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-(2-Fluorophenyl)-1H-pyrrol-2-yl]methanol >97%
1g
$ 487.00

Matrix Scientific
[1-(2-Fluorophenyl)-1H-pyrrol-2-yl]methanol >97%
500mg
$ 390.00

Crysdot
(1-(2-Fluorophenyl)-1H-pyrrol-2-yl)methanol 95+%
1g
$ 338.00

American Custom Chemicals Corporation
[1-(2-FLUOROPHENYL)-1H-PYRROL-2-YL]METHANOL 95.00%
5MG
$ 495.53

AK Scientific
[1-(2-Fluorophenyl)-1H-pyrrol-2-yl]methanol
500mg
$ 576.00

Total 2 raw suppliers

Chemical Property of [1-(2-fluorophenyl)-1H-pyrrol-2-yl]methanol

Chemical Property:

PSA：25.16000
LogP:2.10870
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:191.074642105
Heavy Atom Count:14
Complexity:188

Purity/Quality:

99% ^*data from raw suppliers

[1-(2-Fluorophenyl)-1H-pyrrol-2-yl]methanol >97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)N2C=CC=C2CO)F

Technology Process of [1-(2-fluorophenyl)-1H-pyrrol-2-yl]methanol

There total 3 articles about [1-(2-fluorophenyl)-1H-pyrrol-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: 100.0%

: 132407-65-9
N-(2-fluorophenyl)pyrrole-2-carboxaldehyde

: 132407-66-0
N-(2-fluorophenyl)-2-hydroxymethylpyrrole

Guidance literature:: With sodium tetrahydroborate; In methanol; at 20 ℃; for 0.5h;
DOI:10.1016/S0040-4020(99)00224-0

Reference yield:

: 89096-77-5
1-(2-fluorophenyl)-1H-pyrrole

: 132407-66-0
N-(2-fluorophenyl)-2-hydroxymethylpyrrole

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / POCl₃ / 3 h / 50 °C

2: 100 percent / NaBH₄ / methanol / 0.5 h / 20 °C

With sodium tetrahydroborate; trichlorophosphate; In methanol; 1: Vilsmeier-Haak formylation / 2: Reduction;
DOI:10.1016/S0040-4020(99)00224-0

Reference yield:

: 348-54-9
2-Fluoroaniline

: 132407-66-0
N-(2-fluorophenyl)-2-hydroxymethylpyrrole

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / acetic acid / 1 h / Heating

2: 85 percent / POCl₃ / 3 h / 50 °C

3: 100 percent / NaBH₄ / methanol / 0.5 h / 20 °C

With sodium tetrahydroborate; trichlorophosphate; In methanol; acetic acid; 1: Condensation / 2: Vilsmeier-Haak formylation / 3: Reduction;
DOI:10.1016/S0040-4020(99)00224-0