[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane

[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane Suppliers list
Company Name: Shanghai Daken Advanced Materials Co.,Ltd
Tel: +86-371-66670886
Email: info@dakenam.com
Products Intro: Product Name:[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane
CAS:536975-50-5
Purity:99% Package:1KG,5KG 10KG
Company Name: ANHUI WITOP BIOTECH CO., LTD
Tel: +8615255079626
Email: eric@witopchemical.com
Products Intro: Product Name:[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane
CAS:536975-50-5
Company Name: Amadis Chemical Company Limited
Tel: 571-89925085
Email: sales@amadischem.com
Products Intro: Product Name:[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane
CAS:536975-50-5
Purity:0.97 Package:mgs,gs,kgs Remarks:A854384
Company Name: J & K SCIENTIFIC LTD.  
Tel: 010-82848833 400-666-7788
Email: jkinfo@jkchemical.com
Products Intro: Product Name:[Difluoro(phenylsulfonyl)methyl]trimethylsilane, 98%
CAS:536975-50-5
Purity:98% Package:1G
Company Name: Daicel Chiral Technologies (China)CO.,LTD  
Tel: 021-50460086-9 15921403865
Email: han_yajun@dctc.daicel.com
Products Intro: Product Name:Difluoro(trimethylsilyl)methyl]sulfonyl]-benzene
CAS:536975-50-5
Purity:95%/98% Package:1G;100G; 1KG Remarks:201210
[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane Basic information
Product Name:[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane
Synonyms:[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane;Difluoro(trimethylsilyl)methyl]sulfonyl]-benzene;Benzene, [[difluoro(trimethylsilyl)methyl]sulfonyl]-
CAS:536975-50-5
MF:C10H14F2O2SSi
MW:264.36
EINECS:
Product Categories:
Mol File:536975-50-5.mol
[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane Structure
[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane Chemical Properties
Boiling point 96-97 °C(Press: 1 Torr)
density 1.162±0.06 g/cm3(Predicted)
Safety Information
Safety Statements 24/25
HS Code 29350090
MSDS Information
[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane Usage And Synthesis
DescriptionA much milder difluoro(phenylsulfonyl)methylation reagent than difluoromethyl phenyl sulfone. Under the action of Lewis bases such as such as tetrabutylammonium triphenyldifluorosilicate (TBAT), potassium fluoride, potassium hydrodifluoride, and potassium carbonate, difluoro(phenylsulfonyl)methyl can be transferred to aldehydes, ketones, alkyl halides, and non-activated imines.
Reactions(1) Difluoromethylation of aldehydes and ketones.
Difluoromethylation of aldehydes and ketones.
(2) Difluoromethylation of alkyl halides.
Difluoromethylation of alkyl halides
(3) Difluoromethylation of imines and enamines.
Difluoromethylation of imines and enamines
References[1] H. TOMIOKA. Selective oxidation of a primary hydroxyl in the presence of secondary one[J]. Tetrahedron Letters, 1981, 49 1: 1605-1608. DOI:10.1016/S0040-4039(01)90389-2
[2] LINGUI ZHU. Nucleophilic (phenylsulfonyl)difluoromethylation of alkyl halides using PhSO2CF2SiMe3: preparation of gem-difluoroalkenes and trifluoromethyl compounds[J]. Tetrahedron Letters, 2010, 51 47: Pages 6150-6152. DOI:10.1016/j.tetlet.2010.09.068.
[3] MIKHAIL D. KOSOBOKOV. Reactions of Sulfur- and Phosphorus-Substituted Fluoroalkylating Silicon Reagents with Imines and Enamines under Acidic Conditions[J]. The Journal of Organic Chemistry, 2012, 77 4: 2080-2086. DOI:10.1021/jo202669w.
[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane Preparation Products And Raw materials
Preparation ProductsDifluoroiodoMethyl phenyl sulfone
Tag:[difluoro(phenylsulfonyl)Methyl]triMethyl-Silane(536975-50-5) Related Product Information