1,1,3,3-Tetramethyl-2-(phenylsulfanyl)-2,3-dihydro-1H-indene

Base Information

Chemical Name:1,1,3,3-Tetramethyl-2-(phenylsulfanyl)-2,3-dihydro-1H-indene
CAS No.:95447-90-8
Molecular Formula:C₁₉H₂₂S
Molecular Weight:282.45
Hs Code.:
DSSTox Substance ID:DTXSID40537249
Wikidata:Q82412192

Synonyms:95447-90-8;DTXSID40537249;1,1,3,3-Tetramethyl-2-(phenylsulfanyl)-2,3-dihydro-1H-indene

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Supply Marketing:

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

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Chemical Property of 1,1,3,3-Tetramethyl-2-(phenylsulfanyl)-2,3-dihydro-1H-indene

Chemical Property:

XLogP3:6.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:282.14422188
Heavy Atom Count:20
Complexity:314

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1(C(C(C2=CC=CC=C21)(C)C)SC3=CC=CC=C3)C

Technology Process of 1,1,3,3-Tetramethyl-2-(phenylsulfanyl)-2,3-dihydro-1H-indene

There total 2 articles about 1,1,3,3-Tetramethyl-2-(phenylsulfanyl)-2,3-dihydro-1H-indene 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%

: 74768-58-4
1,1,3,3-tetramethylindan-2-thione

: 591-51-5
phenyllithium

: 95447-90-8
1,1,3,3-tetramethyl-2-indanyl phenyl sulfide

: 95447-88-4
1,1,3,3-tetramethyl-2-phenyl-2-indanethiol

Guidance literature:: In diethyl ether; Ambient temperature;
DOI:10.1016/S0040-4039(01)81548-3

Reference yield:

: 74768-84-6
1,1,3,3-tetramethylindane-2-one hydrazone

: 95447-90-8
1,1,3,3-tetramethyl-2-indanyl phenyl sulfide

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / S₂Cl₂ / benzene

2: 24 percent / diethyl ether / 4 h / Ambient temperature

With disulfur dichloride; In diethyl ether; benzene;
DOI:10.1246/bcsj.61.861