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Butane, 1-[(trifluoromethyl)thio]-, also known as 1-(trifluoromethylthio)butane or 1-(CF3S)-butane, is an organic compound with the chemical formula C4H9SF3. It is a colorless, flammable liquid with a pungent odor. Butane, 1-[(trifluoromethyl)thio]- is a derivative of butane, where one hydrogen atom is replaced by a trifluoromethylthio group (CF3S). It is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential toxicity, it is essential to handle Butane, 1-[(trifluoromethyl)thio]- with proper safety measures and in accordance with relevant regulations.

7412-26-2

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7412-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7412-26-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,1 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7412-26:
(6*7)+(5*4)+(4*1)+(3*2)+(2*2)+(1*6)=82
82 % 10 = 2
So 7412-26-2 is a valid CAS Registry Number.

7412-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(trifluoromethylsulfanyl)butane

1.2 Other means of identification

Product number -
Other names Trifluormethyl-n-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:7412-26-2 SDS

7412-26-2Downstream Products

7412-26-2Relevant academic research and scientific papers

Single electron transfer catalyzed simultaneous cleavage of C-S and S-S bonds

Munavalli, S.,Rossman, D. I.,Rohrbaugh, D. K.,Ferguson, C. P.,Banks, H. D.

, p. 85 - 91 (2007/10/02)

Since the S-S bond of polysulfides plays a vital role in biological processes, the chemistry of the S-S bond has attracted considerable attention.The reaction of bis-(trifluoromethyl) trisulfide with organolithium reagents at -78 deg C has now been found to cause simultaneous scissions of the C-S and S-S bonds and to furnish mixed monosulfides, disulfides and trisulfides containing the trifluoromethyl moiety.The formation of the various products has been rationalized on the basis of the involvement of the single electron transfer process.

Process for the preparation of perhaloalkylthioethers

-

, (2008/06/13)

The present invention relates to a process for the preparation of perhaloalkylthioethers by bringing a perhaloalkyl halide, preferably a bromide or an iodide, into contact with a disulphide in the presence of zinc and of sulphur dioxide or of a dithionite or of a hydroxymethanesulphinate or of a formate anion and sulphur dioxide.

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