Cas 1122065-52-4,2-(2',4',5'-trimethylbiphenyl-4-yl)-6-(2,4,5-trimethylphenyl)naphthalene

1122065-52-4

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Basic information

Product Name: 2-(2',4',5'-trimethylbiphenyl-4-yl)-6-(2,4,5-trimethylphenyl)naphthalene
Synonyms: 2-(2',4',5'-trimethylbiphenyl-4-yl)-6-(2,4,5-trimethylphenyl)naphthalene
CAS NO:1122065-52-4
Molecular Formula:
Molecular Weight: 440.628
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-(2',4',5'-trimethylbiphenyl-4-yl)-6-(2,4,5-trimethylphenyl)naphthalene(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2',4',5'-trimethylbiphenyl-4-yl)-6-(2,4,5-trimethylphenyl)naphthalene(1122065-52-4)
EPA Substance Registry System: 2-(2',4',5'-trimethylbiphenyl-4-yl)-6-(2,4,5-trimethylphenyl)naphthalene(1122065-52-4)

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: 1122065-52-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1122065-52-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,2,0,6 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1122065-52:
(9*1)+(8*1)+(7*2)+(6*2)+(5*0)+(4*6)+(3*5)+(2*5)+(1*2)=94
94 % 10 = 4
So 1122065-52-4 is a valid CAS Registry Number.

1122065-52-4Upstream product

5469-19-2 1-bromo-2,4,5-trimethylbenzene

1122065-52-4Downstream Products

1122065-52-4Relevant academic research and scientific papers

Cross-coupling of aryl/alkenyl pivalates with organozinc reagents through nickel-catalyzed C-O bond activation under mild reaction conditions

Li, Bi-Jie,Li, Yi-Zhou,Lu, Xing-Yu,Liu, Jia,Guan, Bing-Tao,Shi, Zhang-Jie

, p. 10124 - 10127 (2008)

Finding the right partner: The catalyst system [NiCl2(PCy 3)2] mediates the title transformation with high efficiency and allows aryl-aryl and vinyl-aryl coupling to proceed. The first example of catalytic cross-coupling u

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