Cas 1609175-01-0,2',2'',4'',6'-tetramethoxy-[1,1':3',1'':3'',1'''-quaterphenyl]-4',6''-diol

1609175-01-0

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Basic information

Product Name: 2',2'',4'',6'-tetramethoxy-[1,1':3',1'':3'',1'''-quaterphenyl]-4',6''-diol
Synonyms: 2',2'',4'',6'-tetramethoxy-[1,1':3',1'':3'',1'''-quaterphenyl]-4',6''-diol
CAS NO:1609175-01-0
Molecular Formula:
Molecular Weight: 458.511
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'',6'-tetramethoxy-[1,1':3',1'':3'',1'''-quaterphenyl]-4',6''-diol(CAS DataBase Reference)
NIST Chemistry Reference: 2',2'',4'',6'-tetramethoxy-[1,1':3',1'':3'',1'''-quaterphenyl]-4',6''-diol(1609175-01-0)
EPA Substance Registry System: 2',2'',4'',6'-tetramethoxy-[1,1':3',1'':3'',1'''-quaterphenyl]-4',6''-diol(1609175-01-0)

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: 1609175-01-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609175-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,1,7 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1609175-01:
(9*1)+(8*6)+(7*0)+(6*9)+(5*1)+(4*7)+(3*5)+(2*0)+(1*1)=160
160 % 10 = 0
So 1609175-01-0 is a valid CAS Registry Number.

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1609175-01-0Relevant academic research and scientific papers

Selective oxidative homo-and cross-coupling of phenols with aerobic catalysts

Lee, Young Eun,Cao, Trung,Torruellas, Carilyn,Kozlowski, Marisa C.

, p. 6782 - 6785 (2014/06/09)

Simple catalysts that use atom-economical oxygen as the terminal oxidant to accomplish selective ortho-ortho, ortho-para, or para-para homo-couplings of phenols are described. In addition, chromium salen catalysts have been discovered as uniquely effective in the cross-coupling of different phenols with high chemo-and regioselectivity.

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