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Propane, 2-methyl-2-[(trifluoromethyl)thio]-, also known as 2-methyl-2-(trifluoromethylthio)propane or 2-(trifluoromethylthio)-2-methylpropane, is an organic compound with the chemical formula C4H9SF3. It is a colorless, flammable liquid with a molecular weight of 150.17 g/mol. Propane, 2-methyl-2-[(trifluoromethyl)thio]- is characterized by the presence of a propane chain with a methyl group at the second carbon and a trifluoromethylthio group attached to the same carbon. The trifluoromethylthio group consists of a sulfur atom bonded to a methyl group, which in turn is bonded to three fluorine atoms. This chemical is primarily used as a precursor in the synthesis of various pharmaceuticals and agrochemicals, as well as a reagent in organic synthesis. Due to its potential reactivity and flammability, it is important to handle Propane, 2-methyl-2-[(trifluoromethyl)thio]- with care and in accordance with proper safety protocols.

2708-84-1

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2708-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2708-84-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,0 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2708-84:
(6*2)+(5*7)+(4*0)+(3*8)+(2*8)+(1*4)=91
91 % 10 = 1
So 2708-84-1 is a valid CAS Registry Number.

2708-84-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-2-[(trifluoromethyl)thio]propane

1.2 Other means of identification

Product number -
Other names Trifluormethyl-tert.-butyl-sulfid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2708-84-1 SDS

2708-84-1Downstream Products

2708-84-1Relevant academic research and scientific papers

Synthetic Uses of Thio- and Selenoesters of Trifluoromethylated Acids. 1. Preparation of Trifluoromethyl Sulfides and Selenides

Billard, Thierry,Roques, Nicolas,Langlois, Bernard R.

, p. 3813 - 3820 (2007/10/03)

Trifluorothioacetates (CF3CO-S-R, from (CF3CO)2O and thiols) as well as trifluoromethanethio-or trifluoromethaneselenosulfonates (CF3SO2-Y-R; Y = S, Se; from CF3SO2Na, RYYR, and Br2) can be formally decarbonylated or desulfonylated, respectively, provided that they are photolyzed at 40°C in the presence of 1 equiv of the corresponding disulfide or diselenide. Trifluoromethyl sulfides or selenides are obtained, and the added disulfide (or diselenide) is recovered after reaction. In such a way, S-(trifluoromethyl)cysteine derivatives can be obtained.

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