Cas 140476-01-3,2-Propenoic acid, 2,3-difluoro-3-[2,3,4,6-tetrafluoro-5-(trifluoromethyl)phenyl]-

140476-01-3

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Basic information

Product Name: 2-Propenoic acid, 2,3-difluoro-3-[2,3,4,6-tetrafluoro-5-(trifluoromethyl)phenyl]-
Synonyms:
CAS NO:140476-01-3
Molecular Formula: C10HF9O2
Molecular Weight: 324.102
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-Propenoic acid, 2,3-difluoro-3-[2,3,4,6-tetrafluoro-5-(trifluoromethyl)phenyl]-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Propenoic acid, 2,3-difluoro-3-[2,3,4,6-tetrafluoro-5-(trifluoromethyl)phenyl]-(140476-01-3)
EPA Substance Registry System: 2-Propenoic acid, 2,3-difluoro-3-[2,3,4,6-tetrafluoro-5-(trifluoromethyl)phenyl]-(140476-01-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 140476-01-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 140476-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,4,7 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 140476-01:
(8*1)+(7*4)+(6*0)+(5*4)+(4*7)+(3*6)+(2*0)+(1*1)=103
103 % 10 = 3
So 140476-01-3 is a valid CAS Registry Number.

140476-01-3Upstream product

140476-01-3Downstream Products

140476-01-3Relevant academic research and scientific papers

REACTION OF PERFLUORINATED METHYL- AND ALKENYLBENZENES WITH INORGANIC OXIDES IN THE PRESENCE OF ANTIMONY PENTAFLUORIDE

Karpov, V. M.,Panteleev, I. V.,Platonov, V. E.

, p. 1932 - 1938 (2007/10/02)

A study was carried out on the reaction of perfluorinated toluene, m-xylene, p-xylene, mesitylene, and m-(1-propenyl)toluene with inorganic oxides in the presence of antimony pentafluoride.Depending on the reaction conditions, polyfluorinated acids resulting from the consecutive conversion of trifluoromethyl groups into carboxylic acid groups are obtained after hydrolysis of the reaction mixtures.

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