Cas 875148-51-9,2-Butenedinitrile, 2-[5-[4-[bis(4-butylphenyl)amino]phenyl]-2-methyl-3-thienyl]-3-(5-bromo- 2-methyl-3-thienyl)-, (2Z)-

875148-51-9

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Basic information

Product Name: 2-Butenedinitrile, 2-[5-[4-[bis(4-butylphenyl)amino]phenyl]-2-methyl-3-thienyl]-3-(5-bromo- 2-methyl-3-thienyl)-, (2Z)-
Synonyms:
CAS NO:875148-51-9
Molecular Formula: C40H38BrN3S2
Molecular Weight: 704.798
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: 2-Butenedinitrile, 2-[5-[4-[bis(4-butylphenyl)amino]phenyl]-2-methyl-3-thienyl]-3-(5-bromo- 2-methyl-3-thienyl)-, (2Z)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Butenedinitrile, 2-[5-[4-[bis(4-butylphenyl)amino]phenyl]-2-methyl-3-thienyl]-3-(5-bromo- 2-methyl-3-thienyl)-, (2Z)-(875148-51-9)
EPA Substance Registry System: 2-Butenedinitrile, 2-[5-[4-[bis(4-butylphenyl)amino]phenyl]-2-methyl-3-thienyl]-3-(5-bromo- 2-methyl-3-thienyl)-, (2Z)-(875148-51-9)

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: 875148-51-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 875148-51-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,5,1,4 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 875148-51:
(8*8)+(7*7)+(6*5)+(5*1)+(4*4)+(3*8)+(2*5)+(1*1)=199
199 % 10 = 9
So 875148-51-9 is a valid CAS Registry Number.

875148-51-9Upstream product

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875148-51-9Relevant academic research and scientific papers

Tunable luminescence of new photochromic bisthienylethenes containing triphenylamine

Luo, Qianfu,Sheng, Saihong,Cheng, Saihe,Tian, He

, p. 321 - 326 (2007/10/03)

Two new photochromic 1,2-bisthienylethenes containing triphenylamine were conveniently prepared; large cyclization quantum yields and obvious fluorescent changes regulated by the photoisomerization were observed. The substitution effect on the photochromic process is discussed based on these systems. CSIRO 2005.

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