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1,1,1-trifluoro-N-(1,1,1,3,3,3-hexafluoropropan-2-ylidene)methanesulfinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31340-35-9

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31340-35-9 Usage

Type of Compound

Organofluorine compound

Functional Groups

Sulfinamide derivative, trifluoromethyl group, hexafluoropropylidene group

Usage

Reagent in organic chemistry

Application

Synthesis of fluorine-containing compounds

Stability

High stability

Inertness

High inertness

Utility

Useful in various chemical reactions and as a building block in the development of pharmaceuticals and agrochemicals

Potential Applications

Development of advanced polymers and fluorinated materials in materials science

Check Digit Verification of cas no

The CAS Registry Mumber 31340-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,3,4 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 31340-35:
(7*3)+(6*1)+(5*3)+(4*4)+(3*0)+(2*3)+(1*5)=69
69 % 10 = 9
So 31340-35-9 is a valid CAS Registry Number.

31340-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3aR,9bR)-6-hydroxy-7,8-dimethoxy-2-propyl-2,3,3a,9b-tetrahydrofuro[3,2-c]isochromen-5-one

1.2 Other means of identification

Product number -
Other names Trifluoromethylsulfenyl bromide

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:31340-35-9 SDS

31340-35-9Downstream Products

31340-35-9Relevant academic research and scientific papers

Sulfur(VI)-oxide-chloride-imides and Sulfur(VI)-oxide-fluoride-imides

Mews, Ruediger,Kricke, Peter,Stahl, Ingo

, p. 1093 - 1098 (2007/10/02)

At room temperature in the presence of CsF sulfur-oxide-chloride-fluoride-imides RfNSOFCl (8) (Rf = CF3, C2F5, i-C3F7, C6F5) are formed from N-perfluoroalkyl-sulfinyl-imides and Cl2.At prolonged reaction times or higher temperatures the chloride is exchanged and the difluorides RfNSOF2 are isolated in high yields.In the same way (CF3)2CFNS(O)ClCF3 (12) and (CF3)2CClNS(O)ClCF3 (13) are obtained from (CF3)2C=N-S(O)CF3 (9) and Cl2/CsF. 12 can be fluorinated by CsF to give (CF3)2CFNS(O)FCF3 (14). 14 is also observed, when fluorine is added to 9 via XeF2 in the presence of BF3, but mainly C-S bond cleavage occurs.SF5NS(O)FCF(CF3)2 (19) was identified by spectroscopic methods from the reaction of SF5NSOF2 and CF3CF=CF2 in the presence of CsF. - Keywords: Sulfinyl-imides, Sulfur-oxide-chloride-fluoride-imides

Hexafluoropropylideniminolithium reactions with halides

Swindell, Richard F.,Babb, Daniel P.,Ouellette, Thomas J.,Shreeve, Jean'ne M.

, p. 242 - 245 (2008/10/08)

Substitution of the hexafluoroisopropylidenimino group for chlorine or fluorine occurs readily when the lithium salt of (CF3)2C=NH is reacted with inorganic compounds of groups IIIa-VIa. The formation of lithium halide prevents nucle

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