2-(Bromomethyl)phenol

Base Information

Chemical Name:2-(Bromomethyl)phenol
CAS No.:58402-38-3
Molecular Formula:C7H7 Br O
Molecular Weight:187.036
Hs Code.:2908199090
DSSTox Substance ID:DTXSID10544748
Nikkaji Number:J2.450.556A
Wikidata:Q82421999
Mol file:58402-38-3.mol

Synonyms:2-(BROMOMETHYL)PHENOL;58402-38-3;BROMOMETHYLPHENOL;SCHEMBL3030014;DTXSID10544748;AKOS006240714;A903702

Suppliers and Price of 2-(Bromomethyl)phenol

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-(BROMOMETHYL)PHENOL 98.00%
1G
$ 1131.90

Total 17 raw suppliers

Chemical Property of 2-(Bromomethyl)phenol

Chemical Property:

Boiling Point:253.6±15.0 °C(Predicted)
PKA:9.35±0.35(Predicted)
PSA：20.23000
Density:1.593±0.06 g/cm3(Predicted)
LogP:2.28710
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:185.96803
Heavy Atom Count:9
Complexity:85

Purity/Quality:

97% ^*data from raw suppliers

2-(BROMOMETHYL)PHENOL 98.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)CBr)O

Technology Process of 2-(Bromomethyl)phenol

There total 9 articles about 2-(Bromomethyl)phenol 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: 79.0%

: 1058648-87-5
2-[(methoxymethoxy)methyl]phenol

: 58402-38-3
o-hydroxybenzyl bromide

Guidance literature:: With tetrabutylammomium bromide; 1-(n-butyl)-3-methylimidazolium tetrachloroindate; at 135 - 140 ℃; for 0.0916667h; chemoselective reaction; Microwave irradiation; Neat (no solvent);
DOI:10.1016/j.tetlet.2010.04.056

Reference yield: 79.0%

: 1058648-91-1
2-[(ethoxymethoxy)methyl]phenol

: 58402-38-3
o-hydroxybenzyl bromide

Guidance literature:: With tetrabutylammomium bromide; 1-(n-butyl)-3-methylimidazolium tetrachloroindate; at 135 - 140 ℃; for 0.0916667h; chemoselective reaction; Microwave irradiation; Neat (no solvent);
DOI:10.1016/j.tetlet.2010.04.056

Reference yield: 70.0%

: 90-01-7
salicylic alcohol

: 58402-38-3
o-hydroxybenzyl bromide

Guidance literature:: With 1,3,5-trichloro-2,4,6-triazine; sodium bromide; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 24h; chemoselective reaction;
DOI:10.1055/s-0028-1083247