Cas 117906-97-5,(E)-4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Pentadecafluoro-2-(3-methyl-butyl)-dec-2-enoic acid propyl ester

117906-97-5

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Basic information

Product Name: (E)-4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Pentadecafluoro-2-(3-methyl-butyl)-dec-2-enoic acid propyl ester
Synonyms: (E)-4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Pentadecafluoro-2-(3-methyl-butyl)-dec-2-enoic acid propyl ester
CAS NO:117906-97-5
Molecular Formula:
Molecular Weight: 552.324
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: (E)-4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Pentadecafluoro-2-(3-methyl-butyl)-dec-2-enoic acid propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Pentadecafluoro-2-(3-methyl-butyl)-dec-2-enoic acid propyl ester(117906-97-5)
EPA Substance Registry System: (E)-4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Pentadecafluoro-2-(3-methyl-butyl)-dec-2-enoic acid propyl ester(117906-97-5)

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: 117906-97-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 117906-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,9,0 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 117906-97:
(8*1)+(7*1)+(6*7)+(5*9)+(4*0)+(3*6)+(2*9)+(1*7)=145
145 % 10 = 5
So 117906-97-5 is a valid CAS Registry Number.

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117906-97-5Relevant academic research and scientific papers

Transition-Metal Complex Catalyzed Perfluoroalkylation. A Facile Synthesis of Fluorine-Containing Esters by Carbo-Carbonylation of Alkynes and Alkenes

Urata, Hisao,Yugari, Hideki,Fuchikami, Takamasa

, p. 833 - 836 (2007/10/02)

Palladium-catalyzed reaction of perfluoroalkyl iodides with terminal alkynes or alkenes in alcohols under carbon monoxide pressure in the presence of potassium carbonate directly gives β-perfluoroalkyl-substituted alkenoates or alkanoates, respectively.

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