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110003-22-0

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110003-22-0 Usage

Uses

4,5,5-Trifluoropent-4-enoic acid is used in the prearation of polymer electrolyte for lithium ion battery.

Check Digit Verification of cas no

The CAS Registry Mumber 110003-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,0,0 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 110003-22:
(8*1)+(7*1)+(6*0)+(5*0)+(4*0)+(3*3)+(2*2)+(1*2)=30
30 % 10 = 0
So 110003-22-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H5F3O2/c6-3(5(7)8)1-2-4(9)10/h1-2H2,(H,9,10)

110003-22-0SDS

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 4,5,5-Trifluoropent-4-enoic acid

1.2 Other means of identification

Product number -
Other names 4,5,5-TRIFLUOROPENT-4-ENOIC ACID

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:110003-22-0 SDS

110003-22-0Relevant articles and documents

Pesticidal polyhaloalkene derivatives

-

, (2008/06/13)

Polyhaloalkene compounds of the formula: STR1 wherein X is sulfur, oxygen, or nitrogen, Y1 and Y2 are fluorine, Z is hydrogen or the same as Y1 and Y2, and n is 1-4; provided that: (A) when X is sulfur, Z is fluorine and R is thienyl or substituted thienyl, thianaphthyl or substituted thianaphthyl, thiazolinyl or substituted thiazolinyl, oxadiazolyl or substituted oxadiazolyl, 3,4,4-trifluoro-3-butenyloxycarbonylmethyl, thiadiazolyl substituted by halogen or R2 S, wherein R2 is 3,4,4-trifluoro-3-butenyl or R2 is phenylmethyl or phenylthiomethyl each optionally substituted by halogen or nitro; or R is thiadiazolyl substituted by R3, wherein R3 is substituted aryl, arylalkyl, aryloxyalkyl, alkylthio, haloalkylthio, haloarylthio, cyanoalkylthio, arylalkylthio, aryloxyalkylthio, arylthioalkylthio, heterocycloalkylthio, alkenylthio, haloalkenylthio, halocycloalkylalkenylthio, wherein said aryl or heterocyclic groups of R3 may be mono-, di-, tri-, tetra-, or penta-substituted; or R3 is an amino group mono- or di- substituted with members independently selected from alkyl, alkylcarbonyl, haloalkylcarbonyl, aryl, arylaminocarbonyl, arylalkylcarbonyl, arylalkoxycarbonyl, and 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarbonyl; (B) when X is oxygen, Z is fluorine and R is C(O)R1, wherein R1 is perfluoralkyl, phenyl or substituted phenyl, thienyl or substituted thienyl, furanyl or substituted furanyl, pyrollyl or substituted pyrollyl, or dihydrothiazolylthiomethyl; and (C) when X is nitrogen, R taken with the nitrogen is an isothiocyanate, succinimide, or saccharine group. The compounds exhibit activity against plant nematodes and helminths that are indicators of animal anthelmintic activity and therefore are useful in agriculture and veterinary practice.

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