Cas 1159263-90-7,ethyl 4-(3,4',4''-trihexyl-5''-iodo-[2,2',5',2'']terthiophen-5-yl)-benzoate

1159263-90-7

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Basic information

Product Name: ethyl 4-(3,4',4''-trihexyl-5''-iodo-[2,2',5',2'']terthiophen-5-yl)-benzoate
Synonyms: ethyl 4-(3,4',4''-trihexyl-5''-iodo-[2,2',5',2'']terthiophen-5-yl)-benzoate
CAS NO:1159263-90-7
Molecular Formula:
Molecular Weight: 774.935
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: ethyl 4-(3,4',4''-trihexyl-5''-iodo-[2,2',5',2'']terthiophen-5-yl)-benzoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 4-(3,4',4''-trihexyl-5''-iodo-[2,2',5',2'']terthiophen-5-yl)-benzoate(1159263-90-7)
EPA Substance Registry System: ethyl 4-(3,4',4''-trihexyl-5''-iodo-[2,2',5',2'']terthiophen-5-yl)-benzoate(1159263-90-7)

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: 1159263-90-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1159263-90-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,9,2,6 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1159263-90:
(9*1)+(8*1)+(7*5)+(6*9)+(5*2)+(4*6)+(3*3)+(2*9)+(1*0)=167
167 % 10 = 7
So 1159263-90-7 is a valid CAS Registry Number.

1159263-90-7Upstream product

1159263-93-0 C₃₉H₅₁BrO₂S₃

1159263-90-7Downstream Products

1159263-94-1 C₄₉H₆₅BrO₂S₄

1159263-90-7Relevant academic research and scientific papers

Stepwise construction of head-to-tail-type oligothiophenes via iterative palladium-catalyzed CH arylation and halogen exchange

Masuda, Naoyuki,Tanba, Shunsuke,Sugie, Atsushi,Monguchi, Daiki,Koumura, Nagatoshi,Hara, Kohjiro,Mori, Atsunori

scheme or table, p. 2297 - 2300 (2009/10/02)

The well-defined head-to-tail oligothiophenes were synthesized via palladium-catalyzed CH arylation and halogen exchange sequentially through the 2-halothiophene derivatives.

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