Cas 915031-22-0,4-{4'-[2-(5'-chloro-5-methyl-[2,2']bithiophenyl-4-yl)-cyclopent-1-enyl]-5'-methyl-[2,2']bithiophenyl-5-yl}-benzaldehyde

915031-22-0

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Basic information

Product Name: 4-{4'-[2-(5'-chloro-5-methyl-[2,2']bithiophenyl-4-yl)-cyclopent-1-enyl]-5'-methyl-[2,2']bithiophenyl-5-yl}-benzaldehyde
Synonyms:
CAS NO:915031-22-0
Molecular Formula:
Molecular Weight: 563.229
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: 4-{4'-[2-(5'-chloro-5-methyl-[2,2']bithiophenyl-4-yl)-cyclopent-1-enyl]-5'-methyl-[2,2']bithiophenyl-5-yl}-benzaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 4-{4'-[2-(5'-chloro-5-methyl-[2,2']bithiophenyl-4-yl)-cyclopent-1-enyl]-5'-methyl-[2,2']bithiophenyl-5-yl}-benzaldehyde(915031-22-0)
EPA Substance Registry System: 4-{4'-[2-(5'-chloro-5-methyl-[2,2']bithiophenyl-4-yl)-cyclopent-1-enyl]-5'-methyl-[2,2']bithiophenyl-5-yl}-benzaldehyde(915031-22-0)

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: 915031-22-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 915031-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,0,3 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 915031-22:
(8*9)+(7*1)+(6*5)+(5*0)+(4*3)+(3*1)+(2*2)+(1*2)=130
130 % 10 = 0
So 915031-22-0 is a valid CAS Registry Number.

915031-22-0Upstream product

915031-22-0Downstream Products

915031-24-2 C₇₂H₅₄Cl₂N₂S₁₀

915031-22-0Relevant academic research and scientific papers

Photochromic thiophene oligomers based on bisthienylethene: Syntheses, photochromic and two-photon properties

Feng, Yanli,Yan, Yongli,Wang, Sheng,Zhu, Weihong,Qian, Shixiong,Tian, He

, p. 3685 - 3692 (2006)

A series of novel, functional symmetric and unsymmetric photochromic thiophene oligomers based on bisthienylethenes (BTEs) were synthesized via control of the reaction condition with a Suzuki coupling method. Their optical, photochromic quantum yields, tw

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