Benzoyl chloride, 3,5-bis[(trimethylsilyl)oxy]-

Base Information

Chemical Name:Benzoyl chloride, 3,5-bis[(trimethylsilyl)oxy]-
CAS No.:75750-29-7
Molecular Formula:C13H21ClO3Si2
Molecular Weight:316.932
Hs Code.:
DSSTox Substance ID:DTXSID40473875
Nikkaji Number:J680.152H
Wikidata:Q82303547

Synonyms:Benzoyl chloride, 3,5-bis[(trimethylsilyl)oxy]-;75750-29-7;3,5-bis(trimethylsiloxy)benzoyl chloride;SCHEMBL3519634;DTXSID40473875

Suppliers and Price of Benzoyl chloride, 3,5-bis[(trimethylsilyl)oxy]-

Supply Marketing:

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

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Chemical Property of Benzoyl chloride, 3,5-bis[(trimethylsilyl)oxy]-

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:316.0717753
Heavy Atom Count:19
Complexity:299

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[Si](C)(C)OC1=CC(=CC(=C1)C(=O)Cl)O[Si](C)(C)C

Technology Process of Benzoyl chloride, 3,5-bis[(trimethylsilyl)oxy]-

There total 2 articles about Benzoyl chloride, 3,5-bis[(trimethylsilyl)oxy]- 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: 65.0%

: 79314-27-5
3,5-bis(trimethylsiloxy)benzoic acid trimethylsilyl ester

: 75750-29-7
3,5-bis(trimethylsilyloxyl)benzoyl chloride

Guidance literature:: With thionyl chloride; trimethylamine hydrochloride; In dichloromethane; for 3h; Heating;
DOI:10.1021/ja00012a030

Reference yield:

: 99-10-5
3,5-Dihydroxybenzoic acid

: 75750-29-7
3,5-bis(trimethylsilyloxyl)benzoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / triethylamine / toluene / 2 h / Heating

2: 50 percent / SOCl₂ / CH₂Cl₂ / 3 h / Heating

With thionyl chloride; triethylamine; In dichloromethane; toluene;