Cas 339985-37-4,Benzenamine, 4-[2,2':5',2''-terthiophen]-5-yl-N,N-bis(4-[2,2':5',2''-terthiophen]-5-ylphen yl)-

339985-37-4

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Basic information

Product Name: Benzenamine, 4-[2,2':5',2''-terthiophen]-5-yl-N,N-bis(4-[2,2':5',2''-terthiophen]-5-ylphen yl)-
Synonyms:
CAS NO:339985-37-4
Molecular Formula: C54H33NS9
Molecular Weight: 984.457
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: Benzenamine, 4-[2,2':5',2''-terthiophen]-5-yl-N,N-bis(4-[2,2':5',2''-terthiophen]-5-ylphen yl)-(CAS DataBase Reference)
NIST Chemistry Reference: Benzenamine, 4-[2,2':5',2''-terthiophen]-5-yl-N,N-bis(4-[2,2':5',2''-terthiophen]-5-ylphen yl)-(339985-37-4)
EPA Substance Registry System: Benzenamine, 4-[2,2':5',2''-terthiophen]-5-yl-N,N-bis(4-[2,2':5',2''-terthiophen]-5-ylphen yl)-(339985-37-4)

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: 339985-37-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 339985-37-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,9,8 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 339985-37:
(8*3)+(7*3)+(6*9)+(5*9)+(4*8)+(3*5)+(2*3)+(1*7)=204
204 % 10 = 4
So 339985-37-4 is a valid CAS Registry Number.

339985-37-4Upstream product

339985-37-4Downstream Products

339985-37-4Relevant academic research and scientific papers

Synthesis and electrochemical properties of oligo- and poly(thienylphenylamine)s

Yamamoto, Kimihisa,Higuchi, Masayoshi,Uchida, Kumiko,Kojima, Yojiro

, p. 5782 - 5788 (2002)

The oxidative polymerization of tris(thienylphenyl)amine derivatives was performed in acetonitrile by electrochemical and chemical methods. Oligomers were synthesized by stepwise coupling using coupling reactions. The polymer prepared using the trifunctio

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