3-Methyl-2,3-dihydro-1-benzothiophene

Base Information

Chemical Name:3-Methyl-2,3-dihydro-1-benzothiophene
CAS No.:6383-15-9
Molecular Formula:C9H10S
Molecular Weight:150.244
Hs Code.:
DSSTox Substance ID:DTXSID30342869
Nikkaji Number:J2.113.874F

Synonyms:6383-15-9;3-Methyl-2,3-dihydro-1-benzothiophene;Benzo[b]thiophene, 2,3-dihydro-3-methyl-;SCHEMBL12156616;DTXSID30342869;3-methyl-2,3-dihydrobenzothiophene;2,3-Dihydro-3-methylbenzo[b]thiophene;benzo[b]thiophene,2,3-dihydro-3-methyl-;3-Methyl-2,3-dihydro-1-benzothiophene #

Suppliers and Price of 3-Methyl-2,3-dihydro-1-benzothiophene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of 3-Methyl-2,3-dihydro-1-benzothiophene

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:150.05032149
Heavy Atom Count:10
Complexity:122

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1CSC2=CC=CC=C12

Technology Process of 3-Methyl-2,3-dihydro-1-benzothiophene

There total 2 articles about 3-Methyl-2,3-dihydro-1-benzothiophene 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: 88.0%

: 154180-30-0
allyl (2-bromophenyl) thioether

: 6383-15-9
3-methyl-2,3-dihydrobenzo[b]thiophene

: 5296-64-0
allyl phenyl thioether

Guidance literature:: With 2-H-1,3-di-tert-butyl-1,3,2-diazaphosphorinane; 2,2'-azobis(isobutyronitrile); In toluene; at 90 ℃; for 8h; chemoselective reaction;
DOI:10.1039/d0sc01352h