(4-Bromo-2,5-dimethoxyphenyl)methanol

Base Information

Chemical Name:(4-Bromo-2,5-dimethoxyphenyl)methanol
CAS No.:87050-61-1
Molecular Formula:C9H11BrO3
Molecular Weight:247.089
Hs Code.:2909499000
DSSTox Substance ID:DTXSID30588104
Wikidata:Q82480603

Synonyms:(4-BROMO-2,5-DIMETHOXYPHENYL)METHANOL;87050-61-1;SCHEMBL24765332;DTXSID30588104;MFCD08442139;AKOS000124862;AB87740;CS-0194203;E90132

Suppliers and Price of (4-Bromo-2,5-dimethoxyphenyl)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

Crysdot
(4-Bromo-2,5-dimethoxyphenyl)methanol 95+%
1g
$ 377.00

Chemenu
(4-bromo-2,5-dimethoxyphenyl)methanol 95%
1g
$ 356.00

AOBChem
(4-Bromo-2,5-dimethoxyphenyl)methanol 97%
25g
$ 3096.00

American Custom Chemicals Corporation
(4-BROMO-2,5-DIMETHOXYPHENYL)METHANOL 98.00%
10G
$ 1865.33

Alichem
(4-Bromo-2,5-dimethoxyphenyl)methanol
1g
$ 323.40

ACHEMBLOCK
(4-Bromo-2,5-dimethoxyphenyl)methanol 95%
5G
$ 1205.00

ACHEMBLOCK
(4-Bromo-2,5-dimethoxyphenyl)methanol 95%
1G
$ 335.00

Total 8 raw suppliers

Chemical Property of (4-Bromo-2,5-dimethoxyphenyl)methanol

Chemical Property:

Boiling Point:335.0±37.0 °C(Predicted)
PKA:13.77±0.10(Predicted)
PSA：38.69000
Density:1.475±0.06 g/cm3(Predicted)
LogP:1.95860
Storage Temp.:2-8°C
XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:245.98916
Heavy Atom Count:13
Complexity:154

Purity/Quality:

98%+ ^*data from raw suppliers

(4-Bromo-2,5-dimethoxyphenyl)methanol 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=C(C=C1CO)OC)Br

Technology Process of (4-Bromo-2,5-dimethoxyphenyl)methanol

There total 3 articles about (4-Bromo-2,5-dimethoxyphenyl)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%

: 31558-41-5
4-bromo-2,5-dimethoxybenzaldehyde

: 87050-61-1
(4-bromo-2,5-dimethoxy-phenyl)-methanol

Guidance literature:: With sodium tetrahydroborate; In methanol; at 0 - 20 ℃;
DOI:10.1021/ja016585u

Reference yield:

: 2674-34-2
1,4-dibromo-2,5-dimethoxybenzene

: 87050-61-1
(4-bromo-2,5-dimethoxy-phenyl)-methanol

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium; DMF / diethyl ether; hexane / 0.42 h / 0 °C

1.2: 81 percent / hexane / 0.17 h / Heating

2.1: 100 percent / sodium borohydride / methanol / 0 - 20 °C

With sodium tetrahydroborate; n-butyllithium; N,N-dimethyl-formamide; In methanol; diethyl ether; hexane;
DOI:10.1021/ja016585u