Cas 201011-62-3,(5-{5-[(3,5-Di-tert-butyl-4-hydroxy-phenyl)-thiophen-2-yl-methyl]-thiophene-2-carbonyl}-thiophen-2-yl)-{5-[(3,5-di-tert-butyl-4-hydroxy-phenyl)-thiophen-2-yl-methyl]-thiophen-2-yl}-methanone

201011-62-3

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Product Name: (5-{5-[(3,5-Di-tert-butyl-4-hydroxy-phenyl)-thiophen-2-yl-methyl]-thiophene-2-carbonyl}-thiophen-2-yl)-{5-[(3,5-di-tert-butyl-4-hydroxy-phenyl)-thiophen-2-yl-methyl]-thiophen-2-yl}-methanone
Synonyms:
CAS NO:201011-62-3
Molecular Formula:
Molecular Weight: 905.344
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: (5-{5-[(3,5-Di-tert-butyl-4-hydroxy-phenyl)-thiophen-2-yl-methyl]-thiophene-2-carbonyl}-thiophen-2-yl)-{5-[(3,5-di-tert-butyl-4-hydroxy-phenyl)-thiophen-2-yl-methyl]-thiophen-2-yl}-methanone(CAS DataBase Reference)
NIST Chemistry Reference: (5-{5-[(3,5-Di-tert-butyl-4-hydroxy-phenyl)-thiophen-2-yl-methyl]-thiophene-2-carbonyl}-thiophen-2-yl)-{5-[(3,5-di-tert-butyl-4-hydroxy-phenyl)-thiophen-2-yl-methyl]-thiophen-2-yl}-methanone(201011-62-3)
EPA Substance Registry System: (5-{5-[(3,5-Di-tert-butyl-4-hydroxy-phenyl)-thiophen-2-yl-methyl]-thiophene-2-carbonyl}-thiophen-2-yl)-{5-[(3,5-di-tert-butyl-4-hydroxy-phenyl)-thiophen-2-yl-methyl]-thiophen-2-yl}-methanone(201011-62-3)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
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Hazardous Substances Data: 201011-62-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 201011-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,0,1 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 201011-62:
(8*2)+(7*0)+(6*1)+(5*0)+(4*1)+(3*1)+(2*6)+(1*2)=43
43 % 10 = 3
So 201011-62-3 is a valid CAS Registry Number.

201011-62-3Upstream product

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201011-62-3Relevant academic research and scientific papers

Oligo(p-quinone methide)s bridged with thiophene rings. Novel oligomeric, quinonoid π-systems with high electron affinity

Kurata, Hiroyuki,Hisamitsu, Akihito,Oda, Masaji

, p. 8875 - 8878 (2007/10/03)

Novel cross-conjugated oligomers composed of p-quinone methides and thiophenes, synthesized up to tetramer, possess substantially high electron affinity (CV). Alkali metal reduction of the dimer yields a stereoisomeric mixture of stable dianions, and protonation with trifluoroacetic acid generates the corresponding monocation and dication depending on acid strength.

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