Cas 85225-65-6,2,2',3,3',5,5',6,6'-octafluoro-4,4'-bis(3-methoxyphenoxy)-1,1'-biphenyl

85225-65-6

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Basic information

Product Name: 2,2',3,3',5,5',6,6'-octafluoro-4,4'-bis(3-methoxyphenoxy)-1,1'-biphenyl
Synonyms: 2,2',3,3',5,5',6,6'-octafluoro-4,4'-bis(3-methoxyphenoxy)-1,1'-biphenyl
CAS NO:85225-65-6
Molecular Formula: C₂₆H₁₄F₈O₄
Molecular Weight: 542.3741856
EINECS: N/A
Product Categories: N/A
Mol File: 85225-65-6.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2,2',3,3',5,5',6,6'-octafluoro-4,4'-bis(3-methoxyphenoxy)-1,1'-biphenyl(CAS DataBase Reference)
NIST Chemistry Reference: 2,2',3,3',5,5',6,6'-octafluoro-4,4'-bis(3-methoxyphenoxy)-1,1'-biphenyl(85225-65-6)
EPA Substance Registry System: 2,2',3,3',5,5',6,6'-octafluoro-4,4'-bis(3-methoxyphenoxy)-1,1'-biphenyl(85225-65-6)

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: 85225-65-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85225-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,2 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85225-65:
(7*8)+(6*5)+(5*2)+(4*2)+(3*5)+(2*6)+(1*5)=136
136 % 10 = 6
So 85225-65-6 is a valid CAS Registry Number.

85225-65-6Upstream product

85225-65-6Downstream Products

85225-67-8 p,p'-bis(3-hydroxyphenoxy)octafluorobiphenyl

85225-65-6Relevant articles and documents

BISPHENOLS BASED ON HEXAFLUOROBENZENE AND DECAFLUOROBIPHENYL

Kameneva, T. M.,Malichenko, B. F.,Shelud'ko, E. V.,Pogorelyi, V. K.,Sherstyuk, A. I.,Rozhenko, A. B.

, p. 518 - 523 (2007/10/02)

The reaction of hexafluorobenzene or decafluorobiphenyl with the monoethyl ethers of hydroquinone, resorcinol and pyrocatechol followed by demethylation of the bismethoxy derivatives led to the formation of the corresponding bisphenols.Some of their physi

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