Cas 1234556-30-9,1-(4-(trifluoromethoxy)phenyl)-2-(trifluoromethylsulfonyloxy)anthraquinone

1234556-30-9

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Basic information

Product Name: 1-(4-(trifluoromethoxy)phenyl)-2-(trifluoromethylsulfonyloxy)anthraquinone
Synonyms: 1-(4-(trifluoromethoxy)phenyl)-2-(trifluoromethylsulfonyloxy)anthraquinone
CAS NO:1234556-30-9
Molecular Formula:
Molecular Weight: 516.374
EINECS: N/A
Product Categories: N/A
Mol File: 1234556-30-9.mol
Article Data: 2

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-(trifluoromethoxy)phenyl)-2-(trifluoromethylsulfonyloxy)anthraquinone(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-(trifluoromethoxy)phenyl)-2-(trifluoromethylsulfonyloxy)anthraquinone(1234556-30-9)
EPA Substance Registry System: 1-(4-(trifluoromethoxy)phenyl)-2-(trifluoromethylsulfonyloxy)anthraquinone(1234556-30-9)

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: 1234556-30-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1234556-30-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,4,5,5 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1234556-30:
(9*1)+(8*2)+(7*3)+(6*4)+(5*5)+(4*5)+(3*6)+(2*3)+(1*0)=139
139 % 10 = 9
So 1234556-30-9 is a valid CAS Registry Number.

1234556-30-9Upstream product

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1234556-30-9Relevant articles and documents

Site-selective arylation of alizarin and purpurin based on Suzuki-Miyaura cross-coupling reactions

Mahal, Ahmed,Villinger, Alexander,Langer, Peter

, p. 2075 - 2087 (2011/05/16)

A variety of arylated anthraquinones were prepared by site-selective Suzuki-Miyaura cross-coupling reactions of the bis- and tris(triflates) of alizarin and purpurin, respectively. The site-selectivity is controlled by the electronic influence of the carb

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