3-Bromo-2-methylbenzofuran

Base Information

Chemical Name:3-Bromo-2-methylbenzofuran
CAS No.:58863-48-2
Molecular Formula:C9H7BrO
Molecular Weight:211.058
Hs Code.:2932990090
European Community (EC) Number:967-439-6
DSSTox Substance ID:DTXSID30467849
Nikkaji Number:J2.800.237H
Wikidata:Q82294925
Mol file:58863-48-2.mol

Synonyms:3-bromo-2-methylbenzofuran;58863-48-2;3-bromo-2-methyl-1-benzofuran;Benzofuran, 3-bromo-2-methyl-;3-bromo-2-mehtylbenzofuran;MFCD11111717;BENZOFURAN,3-BROMO-2-METHYL-;methyl 3-bromo-1-benzofuran;SCHEMBL3380593;DTXSID30467849;OEGMISNFEAVBHA-UHFFFAOYSA-N;AKOS022691250;AS-36540;SY242342;CS-0061201;EN300-5414708

Suppliers and Price of 3-Bromo-2-methylbenzofuran

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

SynQuest Laboratories
3-Bromo-2-methylbenzofuran 97%
250 mg
$ 226.00

Crysdot
3-Bromo-2-methylbenzofuran 97%
1g
$ 434.00

ChemScene
3-Bromo-2-methylbenzofuran >97.0%
1g
$ 371.00

ChemScene
3-Bromo-2-methylbenzofuran >97.0%
100mg
$ 99.00

ChemScene
3-Bromo-2-methylbenzofuran >97.0%
250mg
$ 183.00

Alichem
3-Bromo-2-methylbenzofuran
250mg
$ 165.90

Alichem
3-Bromo-2-methylbenzofuran
1g
$ 413.70

AK Scientific
3-BROMO-2-METHYL-1-BENZOFURAN
1g
$ 683.60

Total 10 raw suppliers

Chemical Property of 3-Bromo-2-methylbenzofuran

Chemical Property:

PSA：13.14000
LogP:3.50370
XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:209.96803
Heavy Atom Count:11
Complexity:149

Purity/Quality:

99.0% ^*data from raw suppliers

3-Bromo-2-methylbenzofuran 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(C2=CC=CC=C2O1)Br

Technology Process of 3-Bromo-2-methylbenzofuran

There total 4 articles about 3-Bromo-2-methylbenzofuran 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: 56.0%

: 4265-25-2
2-methylbenzofuran

: 58863-48-2
3-bromo-2-methyl-1-benzofuran

Guidance literature:: With N-Bromosuccinimide; In tetrahydrofuran; at 5 ℃;

Reference yield:

: 58863-48-2
3-bromo-2-methyl-1-benzofuran

Guidance literature:: With carbon disulfide; bromine; at 0 ℃;

Reference yield:

: 271-89-6
1-benzofurane

: 58863-48-2
3-bromo-2-methyl-1-benzofuran

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 2 h / -78 °C

1.2: 8 h / 20 °C

2.1: N-Bromosuccinimide / tetrahydrofuran / 24 h / 0 - 20 °C

With N-Bromosuccinimide; n-butyllithium; In tetrahydrofuran; hexane;
DOI:10.1039/d0tc01044h