Cas 136365-60-1,<(5-(Trifluoroethenyl)-1,3-phenylene)bis<2,2,2-trifluoro-1-(trifluoromethyl)ethylidene>oxy>bis<trimethylsilane>

136365-60-1

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Basic information

Product Name: <(5-(Trifluoroethenyl)-1,3-phenylene)bis<2,2,2-trifluoro-1-(trifluoromethyl)ethylidene>oxy>bis
Synonyms: <(5-(Trifluoroethenyl)-1,3-phenylene)bis<2,2,2-trifluoro-1-(trifluoromethyl)ethylidene>oxy>bis
CAS NO:136365-60-1
Molecular Formula:
Molecular Weight: 634.533
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: <(5-(Trifluoroethenyl)-1,3-phenylene)bis<2,2,2-trifluoro-1-(trifluoromethyl)ethylidene>oxy>bis(CAS DataBase Reference)
NIST Chemistry Reference: <(5-(Trifluoroethenyl)-1,3-phenylene)bis<2,2,2-trifluoro-1-(trifluoromethyl)ethylidene>oxy>bis(136365-60-1)
EPA Substance Registry System: <(5-(Trifluoroethenyl)-1,3-phenylene)bis<2,2,2-trifluoro-1-(trifluoromethyl)ethylidene>oxy>bis(136365-60-1)

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: 136365-60-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 136365-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,3,6 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 136365-60:
(8*1)+(7*3)+(6*6)+(5*3)+(4*6)+(3*5)+(2*6)+(1*0)=131
131 % 10 = 1
So 136365-60-1 is a valid CAS Registry Number.

136365-60-1Upstream product

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136365-60-1Relevant academic research and scientific papers

THE SYNTHESIS AND ATTEMPTED POLYMERIZATION OF AN α,β,β-TRIFLUOROSTYRENE DISUBSTITUTED BY HEXAFLUORO-2-PROPANOL GROUPS

Sprague, Lee G.,Snow, Arthur W.,Griffith, James R.

, p. 301 - 306 (1991)

The preparation of oxy>-bis 2 in excellent isolated yield from the corresponding aryl iodide 4 is described.The synthesis features conversion of the know

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