Cas 377754-10-4,butyl-dimethyl-(2,3,4,5,6,2',3',5',6'-nonafluoro-[1,1';4',1'';4'',1''']quaterphenyl-4'''-ylethynyl)-silane

377754-10-4

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Basic information

Product Name: butyl-dimethyl-(2,3,4,5,6,2',3',5',6'-nonafluoro-[1,1';4',1'';4'',1''']quaterphenyl-4'''-ylethynyl)-silane
Synonyms: butyl-dimethyl-(2,3,4,5,6,2',3',5',6'-nonafluoro-[1,1';4',1'';4'',1''']quaterphenyl-4'''-ylethynyl)-silane
CAS NO:377754-10-4
Molecular Formula:
Molecular Weight: 606.606
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: butyl-dimethyl-(2,3,4,5,6,2',3',5',6'-nonafluoro-[1,1';4',1'';4'',1''']quaterphenyl-4'''-ylethynyl)-silane(CAS DataBase Reference)
NIST Chemistry Reference: butyl-dimethyl-(2,3,4,5,6,2',3',5',6'-nonafluoro-[1,1';4',1'';4'',1''']quaterphenyl-4'''-ylethynyl)-silane(377754-10-4)
EPA Substance Registry System: butyl-dimethyl-(2,3,4,5,6,2',3',5',6'-nonafluoro-[1,1';4',1'';4'',1''']quaterphenyl-4'''-ylethynyl)-silane(377754-10-4)

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: 377754-10-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 377754-10-4 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, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 377754-10:
(8*3)+(7*7)+(6*7)+(5*7)+(4*5)+(3*4)+(2*1)+(1*0)=184
184 % 10 = 4
So 377754-10-4 is a valid CAS Registry Number.

377754-10-4Upstream product

377754-10-4Downstream Products

377754-11-5 (CCSi(CH₂CH₂CH₂CH₃)(CH₃)2)2(C₆H₄)4(C₆F₄)4(C₆H₂(CH(CH₃)2)2)

377754-10-4Relevant 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 (2001)

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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