Cas 937709-56-3,1,4-Bis-(2-ethyl-hexyloxy)-2-{(E)-2-[4-((E)-2-{4-[(E)-2-(4-iodo-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-vinyl}-5-methyl-benzene

937709-56-3

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Basic information

Product Name: 1,4-Bis-(2-ethyl-hexyloxy)-2-{(E)-2-[4-((E)-2-{4-[(E)-2-(4-iodo-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-vinyl}-5-methyl-benzene
Synonyms: 1,4-Bis-(2-ethyl-hexyloxy)-2-{(E)-2-[4-((E)-2-{4-[(E)-2-(4-iodo-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-vinyl}-5-methyl-benzene
CAS NO:937709-56-3
Molecular Formula:
Molecular Weight: 780.873
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: 1,4-Bis-(2-ethyl-hexyloxy)-2-{(E)-2-[4-((E)-2-{4-[(E)-2-(4-iodo-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-vinyl}-5-methyl-benzene(CAS DataBase Reference)
NIST Chemistry Reference: 1,4-Bis-(2-ethyl-hexyloxy)-2-{(E)-2-[4-((E)-2-{4-[(E)-2-(4-iodo-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-vinyl}-5-methyl-benzene(937709-56-3)
EPA Substance Registry System: 1,4-Bis-(2-ethyl-hexyloxy)-2-{(E)-2-[4-((E)-2-{4-[(E)-2-(4-iodo-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-vinyl}-5-methyl-benzene(937709-56-3)

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: 937709-56-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 937709-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,7,7,0 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 937709-56:
(8*9)+(7*3)+(6*7)+(5*7)+(4*0)+(3*9)+(2*5)+(1*6)=213
213 % 10 = 3
So 937709-56-3 is a valid CAS Registry Number.

937709-56-3Upstream product

937709-56-3Downstream Products

937709-56-3Relevant academic research and scientific papers

Practical Synthesis of Vinyl-Substituted p-Phenylenevinylene Oligomers and Their Triethoxysilyl Derivatives

Sugiono, Erli,Metzroth, Thorsten,Detert, Heiner

, p. 351 - 359 (2007/10/03)

Luminescent semiconducting organic compounds are widely used as active layers in electro-optical devices. Apart from conjugated polymers, monodisperse oligomers also represent attractive materials. The synthesis of stilbenoid oligomers with polymerizable

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