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(2-bromo-1,1,2,2-tetrafluoroethyl)(phenyl)sulfane

CAS No.
83015-33-2
Chemical Name:
(2-bromo-1,1,2,2-tetrafluoroethyl)(phenyl)sulfane
Synonyms
(2-bromo-1,1,2,2-tetrafluoroethyl)(phenyl)sulfane;(2-bromo-1,1,2,2-tetrafluoroethylsulfanyl)benzene;Benzene, [(2-bromo-1,1,2,2-tetrafluoroethyl)thio]-
CBNumber:
CB64189705
Molecular Formula:
C8H5BrF4S
Molecular Weight:
289.09
MDL Number:
MFCD27996155
MOL File:
83015-33-2.mol
Last updated:2025-01-27 09:38:02

(2-bromo-1,1,2,2-tetrafluoroethyl)(phenyl)sulfane Properties

form liquid
UNSPSC Code 12352101
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319-H413
Precautionary statements  P273-P305+P351+P338

(2-bromo-1,1,2,2-tetrafluoroethyl)(phenyl)sulfane price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich CF0014 Phenylsulfanyltetrafluorobromoethane 83015-33-2 1g $645 2024-03-01 Buy
American Custom Chemicals Corporation HCH0418701 (2-BROMO-1,1,2,2-TETRAFLUOROETHYL)(PHENYL)SULFANE 95.00% 83015-33-2 5MG $497.43 2021-12-16 Buy
Product number Packaging Price Buy
CF0014 1g $645 Buy
HCH0418701 5MG $497.43 Buy

(2-bromo-1,1,2,2-tetrafluoroethyl)(phenyl)sulfane Chemical Properties,Uses,Production

Uses

Phenylsulfanyltetrafluoroethyl bromide is a fluoroalkylbromide that is a radical source of the phenylsulfanyltetrafluoroethyl moiety. Alternatively, it can also be selectively metallated at the fluorinated carbon with Turbo Grignard reagent at low temperatures resulting in a thermally unstable anion that can act as a nucleophilic fluoroalkylation reagent towards a wide variety of electrophiles, such as aldehydes, ketones or sulfonylimines. A phenylsulfanyltetrafluoroethyl moiety incorporated in the substrate can be treated with tributyltin hydride and generate the corresponding fluoroalkyl radical. If the substrate lacks any olefins, it can be reduced to tetrafluoroethyl group whereas if the substrate contains an olefin in a correct spatial orientation, it can lead to an intramolecular cyclization affording tetrafluorinated cyclic structures.

reaction suitability

reaction type: C-C Bond Formation

(2-bromo-1,1,2,2-tetrafluoroethyl)(phenyl)sulfane Preparation Products And Raw materials

Raw materials

Preparation Products

(2-bromo-1,1,2,2-tetrafluoroethyl)(phenyl)sulfane Suppliers

Global( 7)Suppliers
Supplier Tel Email Country ProdList Advantage
Bide Pharmatech Ltd. 400-164-7117 13681763483 product02@bidepharm.com China 41457 60
Henan Weituxi Chemical Technology Co., Ltd. 0371-63284658 18135795563 2885349392@qq.com China 9978 58
Dalian Shuanghang Chemical Co., LTD +86-411-66858498 +86-13941194417 sales@dl-bykj.cn China 1977 58
TCI (Shanghai) Chemical Trading Co., Ltd. 021-021-61109150 sales@tcisct.com China 31121 58
Bide Pharmatech Ltd. 400-6005915 sales@picasso-e.com China 39665 58
Merck KGaA 21-20338288 ordercn@merckgroup.com China 292394 58
(2-bromo-1,1,2,2-tetrafluoroethyl)(phenyl)sulfane Benzene, [(2-bromo-1,1,2,2-tetrafluoroethyl)thio]- (2-bromo-1,1,2,2-tetrafluoroethylsulfanyl)benzene 83015-33-2 C8H5BrF4S