6-Chloro-3-methyl-1-benzofuran

Base Information

Chemical Name:6-Chloro-3-methyl-1-benzofuran
CAS No.:30343-35-2
Molecular Formula:C₉H₇ClO
Molecular Weight:166.607
Hs Code.:
DSSTox Substance ID:DTXSID40576214
Wikidata:Q82465788
Mol file:30343-35-2.mol

Synonyms:30343-35-2;6-Chloro-3-methylbenzofuran;6-Chloro-3-methyl-1-benzofuran;Benzofuran, 6-chloro-3-methyl-;MFCD15144093;SCHEMBL2092632;DTXSID40576214;AKOS030587581;AS-9994;SY310488

Suppliers and Price of 6-Chloro-3-methyl-1-benzofuran

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

Total 1 raw suppliers

Chemical Property of 6-Chloro-3-methyl-1-benzofuran

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:166.0185425
Heavy Atom Count:11
Complexity:149

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=COC2=C1C=CC(=C2)Cl

Technology Process of 6-Chloro-3-methyl-1-benzofuran

There total 1 articles about 6-Chloro-3-methyl-1-benzofuran 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: 26.0%

: 30335-94-5
(2-acetyl-5-chlorophenoxy)acetic acid ethyl ester

: 30343-35-2
3-methyl-6-chlorobenzofuran

: 30335-95-6
(2-acetyl-5-chlorophenoxy)acetic acid

: 77956-72-0
8-Chloro-benzo[b]oxepine-3,5-dione

: 81718-75-4
6-Chloro-3-methyl-benzofuran-2-carboxylic acid

Guidance literature:: With potassium hydroxide; In 1,4-dioxane; at 60 ℃; for 6h;

Reference yield:

: 30343-35-2
3-methyl-6-chlorobenzofuran

: 2270-59-9
1-bromo-4-methylpent-3-ene

: 25074-12-8
furoventalene

Guidance literature:: With 1,3-bis[(diphenylphosphino)propane]dichloronickel(II); magnesium; Yield given. Multistep reaction; 1.)Grignard reagent 2.)0 deg C,10 min, then r.t. overnight;