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2,2,3,3,3-PENTAFLUOROPROPYL TRIFLUOROMETHANESULFONATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6401-00-9

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6401-00-9 Usage

General Description

2,2,3,3,3-Pentafluoropropyl trifluoromethanesulfonate is a synthetic organic compound that contains fluorine atoms and a sulfonate group. It is commonly used as a fluorinated solvent in various chemical reactions and as an electrolyte additive in lithium-ion batteries. This chemical has unique properties due to its fluoroalkyl and sulfonate groups, allowing it to be used as a surfactant and in the synthesis of specialty materials. Additionally, 2,2,3,3,3-Pentafluoropropyl trifluoromethanesulfonate is also employed as a reagent in organic synthesis for the modification and functionalization of various substrates. Due to its versatile applications, 2,2,3,3,3-PENTAFLUOROPROPYL TRIFLUOROMETHANESULFONATE is of interest in the field of chemical research and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 6401-00-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,0 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6401-00:
(6*6)+(5*4)+(4*0)+(3*1)+(2*0)+(1*0)=59
59 % 10 = 9
So 6401-00-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H2F8O3S/c5-2(6,3(7,8)9)1-15-16(13,14)4(10,11)12/h1H2

6401-00-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3,3-PENTAFLUOROPROPYL TRIFLUOROMETHANESULFONATE

1.2 Other means of identification

Product number -
Other names 3,3,3,2,2,-pentafluoropropyl trifluoromethanesulfonate

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:6401-00-9 SDS

6401-00-9Relevant academic research and scientific papers

3-(1H-PYRAZOL-4-YL)PYRIDINE ALLOSTERIC MODULATORS OF M4 MUSCARINIC ACETYLCHOLINE RECEPTOR

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Page/Page column 110-111, (2020/05/28)

Provided are cinnolinyl and quinolinyl pyrazol-4-yl-pyridine compounds which are allosteric modulators of the M4 muscarinic acetylcholine receptor, compositions comprising said compounds, and uses of said compounds in the treatment or prevention of diseases in which M4 muscarinic acetylcholine receptors are involved, especially neurological and psychiatric disorders and diseases.

Solvent-free synthesis of alkyl and fluoroalkyl sulfonium salts from sulfides and fluoroalkyl trifluoromethanesulfonates

Song, Hai-Xia,Wang, Shi-Meng,Wang, Xiao-Yan,Han, Jia-Bin,Gao, Ying,Jia, Su-Jiao,Zhang, Cheng-Pan

, p. 131 - 140 (2016/11/19)

A series of diaryl(fluoroalkyl)sulfonium salts were synthesized from electron-rich diaryl sulfides and fluoroalkyl trifluoromethanesulfonates under solvent-free conditions. Unlike diaryl sulfides, dialkyl and alkyl(aryl) sulfides reacted with fluoroalkyl

METALLOENZYME INHIBITOR COMPOUNDS

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Page/Page column 42, (2013/07/31)

The instant invention describes compounds having metalloenzyme modulating activity, and methods of treating diseases, disorders or symptoms thereof mediated by such metalloenzymes.

AMIDINE COMPOUNDS AND USE THEREOF FOR PLANT DISEASE CONTROL

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Page/Page column 127-128, (2012/07/14)

An amidine compound represented by formula (1): wherein R1 represent a C1-C11 fluoroalkyl group, a C3-C11 fluoroalkenyl group or a C3-C11 fluoroalkynyl group; R2 represent a C1-C3 alkyl group; R3 represent a C1-C3 alkyl group; R4 represent a C3-C6 cycloalkyl group or a C1-C6 alkyl group optionally having one or more halogens and R5 represent a C3-C6 cycloalkyl group or a C1-C6 alkyl group optionally having one or more halogens, said compound having excellent plant disease controlling effect.

METALLOENZYME INHIBITOR COMPOUNDS

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Page/Page column 44, (2011/11/06)

The instant invention describes compounds having metalloenzyme modulating activity, and methods of treating diseases, disorders or symptoms thereof mediated by such metalloenzymes.

Preparation of trifluoromethylated ynamines and their reactions with some electrophilic reagents

Ishihara, Takashi,Mantani, Toshiya,Konno, Tsutomu,Yamanaka, Hiroki

, p. 3783 - 3793 (2007/10/03)

N,N-Dialkyl(3,3,3-trifluoro-1-propynyl)amines were prepared by a three-step procedure starting from commercially available 2,2,3,3,3-pentafluoropropanol. The reactions of these trifluoromethylated ynamines with some electrophiles, such as aldehydes, halog

NITRILE COMPOUND AND ITS USE IN PEST CONTROL

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Page/Page column 124, (2010/02/12)

The present invention provides a nitrile compound represented by the formula (I): wherein R represents C1-C4 fluoroalkyl, Q represents halogen, C1-C11 alkyl optionally substituted with halogen, C2-C6 alkenyl group optionally substituted with halogen, C2-C6 alkynyl optionally substituted with halogen, C3-C7 cycloalkyl optionally substituted with halogen or (C3-C7 cycloalkyl optionally substituted with halogen)C1-C4 alkyl, which has excellent control effect against pests.

2,4-DIHYDROXYBENZOIC ACID DERIVATIVES

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Page 29, (2008/06/13)

The present invention relates to novel compounds of formula (I) and to the salts, solvates and prodrugs thereof, wherein the meanings of the various substituents are as disclosed in the description. Said compounds are useful for the treatment or preventio

A new practical and convenient access to the synthesis of N,N-dialkyl-3,3,3-trifluoropropanamides

Yamanaka, Hiroki,Mantani, Toshiya,Shiomi, Keisuke,Ishihara, Takashi

, p. 615 - 616 (2007/10/03)

N,N-Dialkyl-3,3,3-trifluoropropanamides were readily synthesized in good to excellent yields through N,N-dialkyl(3,3,3-trifluoro-1-propynyl)amines, which were generated by the reaction of N,N-dialkyl(2,2,3,3,3-pentafluoropropyl)-or -(2,3,3,3-tetrafluoro-1

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