Cas 1087271-46-2,potassium 2,2,3-trifluoro-3-(1,1,2,2,3,3-hexafluoro-3-trifluoromethoxypropoxy)propionate

1087271-46-2

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Basic information

Product Name: potassium 2,2,3-trifluoro-3-(1,1,2,2,3,3-hexafluoro-3-trifluoromethoxypropoxy)propionate
Synonyms: potassium 2,2,3-trifluoro-3-(1,1,2,2,3,3-hexafluoro-3-trifluoromethoxypropoxy)propionate
CAS NO:1087271-46-2
Molecular Formula:
Molecular Weight: 416.162
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: potassium 2,2,3-trifluoro-3-(1,1,2,2,3,3-hexafluoro-3-trifluoromethoxypropoxy)propionate(CAS DataBase Reference)
NIST Chemistry Reference: potassium 2,2,3-trifluoro-3-(1,1,2,2,3,3-hexafluoro-3-trifluoromethoxypropoxy)propionate(1087271-46-2)
EPA Substance Registry System: potassium 2,2,3-trifluoro-3-(1,1,2,2,3,3-hexafluoro-3-trifluoromethoxypropoxy)propionate(1087271-46-2)

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: 1087271-46-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1087271-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,7,2,7 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1087271-46:
(9*1)+(8*0)+(7*8)+(6*7)+(5*2)+(4*7)+(3*1)+(2*4)+(1*6)=162
162 % 10 = 2
So 1087271-46-2 is a valid CAS Registry Number.

1087271-46-2Upstream product

919005-14-4 2,2,3-trifluoro-3-(1,1,2,2,3,3-hexafluoro-3-trifluoromethoxypropoxy)propionic acid

1087271-46-2Downstream Products

1087271-46-2Relevant academic research and scientific papers

TEMPO mediated oxidation of fluorinated alcohols to carboxylic acids

Ignatowska, Jolanta,Shyshkov, Oleg,Zipplies, Tilman,Hintzer, Klaus,R?schenthaler, Gerd-Volker

, p. 35 - 40 (2012)

Fluorinated carboxylic acids (3a-f) have been prepared in good yield by oxidizing the corresponding alcohols (2a-f) in the presence of TEMPO (1) as catalyst, using oxidants like bleach and oxygen.

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