Acetyl chloride, [(diphenylmethyl)thio]-

Base Information

Chemical Name:Acetyl chloride, [(diphenylmethyl)thio]-
CAS No.:68524-29-8
Molecular Formula:C15H13ClOS
Molecular Weight:276.787
Hs Code.:
DSSTox Substance ID:DTXSID10557095
Wikidata:Q82438859

Synonyms:68524-29-8;[(Diphenylmethyl)sulfanyl]acetyl chloride;SCHEMBL2577789;DTXSID10557095;SRCCYSUDRUXYQJ-UHFFFAOYSA-N;2-[(diphenylmethyl)thio]acetylchloride

Suppliers and Price of Acetyl chloride, [(diphenylmethyl)thio]-

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 Acetyl chloride, [(diphenylmethyl)thio]-

Chemical Property:

XLogP3:4.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:276.0375639
Heavy Atom Count:18
Complexity:239

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(C2=CC=CC=C2)SCC(=O)Cl

Technology Process of Acetyl chloride, [(diphenylmethyl)thio]-

There total 3 articles about Acetyl chloride, [(diphenylmethyl)thio]- 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: 99.9%

: 63547-22-8
(benzhydrylthio)acetic acid

: 68524-29-8
benzhydrylsulfanyl acetyl chloride

Guidance literature:: With thionyl chloride; In benzene; for 1h; Heating;
DOI:10.1016/j.tetasy.2005.07.028

Reference yield:

: 91-01-0
1,1-Diphenylmethanol

: 68524-29-8
benzhydrylsulfanyl acetyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 99.9 percent / SOCl₂ / benzene / 1 h / Heating

With thionyl chloride; In benzene;
DOI:10.1016/j.tetasy.2005.07.028

Reference yield:

: 776-74-9
Bromodiphenylmethane

: 68524-29-8
benzhydrylsulfanyl acetyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: water; acetone / 3 h / 20 - 70 °C / Inert atmosphere

2: thionyl chloride / benzene / 1 h / Inert atmosphere; Reflux

With thionyl chloride; In water; acetone; benzene;