Cas 377754-08-0,4,4'''''-bis-(butyl-dimethyl-silanylethynyl)-2'',3'',5'',6'',2''',3''',5''',6'''-octafluoro-[1,4';1',4'';1'',1''';4''',1'''';4'''',1''''']sexiphenyl

377754-08-0

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Product Name: 4,4'''''-bis-(butyl-dimethyl-silanylethynyl)-2'',3'',5'',6'',2''',3''',5''',6'''-octafluoro-[1,4';1',4'';1'',1''';4''',1'''';4'''',1''''']sexiphenyl
Synonyms: 4,4'''''-bis-(butyl-dimethyl-silanylethynyl)-2'',3'',5'',6'',2''',3''',5''',6'''-octafluoro-[1,4';1',4'';1'',1''';4''',1'''';4'''',1''''']sexiphenyl
CAS NO:377754-08-0
Molecular Formula:
Molecular Weight: 879.095
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: 4,4'''''-bis-(butyl-dimethyl-silanylethynyl)-2'',3'',5'',6'',2''',3''',5''',6'''-octafluoro-[1,4';1',4'';1'',1''';4''',1'''';4'''',1''''']sexiphenyl(CAS DataBase Reference)
NIST Chemistry Reference: 4,4'''''-bis-(butyl-dimethyl-silanylethynyl)-2'',3'',5'',6'',2''',3''',5''',6'''-octafluoro-[1,4';1',4'';1'',1''';4''',1'''';4'''',1''''']sexiphenyl(377754-08-0)
EPA Substance Registry System: 4,4'''''-bis-(butyl-dimethyl-silanylethynyl)-2'',3'',5'',6'',2''',3''',5''',6'''-octafluoro-[1,4';1',4'';1'',1''';4''',1'''';4'''',1''''']sexiphenyl(377754-08-0)

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: 377754-08-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 377754-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,7,7,5 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 377754-08:
(8*3)+(7*7)+(6*7)+(5*7)+(4*5)+(3*4)+(2*0)+(1*8)=190
190 % 10 = 0
So 377754-08-0 is a valid CAS Registry Number.

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377754-08-0Relevant academic research and scientific papers

Efficient, high-yield route to long, functionalized p-phenylene oligomers containing perfluorinated segments, and their cyclodimerizations by zirconocene coupling

Nitschke,Tilley

, p. 10183 - 10190 (2007/10/03)

Linear oligophenylene diynes containing 6, 9, and 12 phenylene rings were synthesized in high yields using the nucleophilic aromatic substitution (SNAr) of perfluoroarenes by aryllithium reagents as the key carbon - carbon bond-forming reaction

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