Cas 200508-07-2,2,2,2-Trifluoro-N-[3-hydroxy-2-(5-hydroxy-1,4-dioxo-1,4-dihydro-naphthalen-2-yl)-5-methyl-phenyl]-acetamide

200508-07-2

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Basic information

Product Name: 2,2,2-Trifluoro-N-[3-hydroxy-2-(5-hydroxy-1,4-dioxo-1,4-dihydro-naphthalen-2-yl)-5-methyl-phenyl]-acetamide
Synonyms:
CAS NO:200508-07-2
Molecular Formula:
Molecular Weight: 391.303
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: 2,2,2-Trifluoro-N-[3-hydroxy-2-(5-hydroxy-1,4-dioxo-1,4-dihydro-naphthalen-2-yl)-5-methyl-phenyl]-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2,2,2-Trifluoro-N-[3-hydroxy-2-(5-hydroxy-1,4-dioxo-1,4-dihydro-naphthalen-2-yl)-5-methyl-phenyl]-acetamide(200508-07-2)
EPA Substance Registry System: 2,2,2-Trifluoro-N-[3-hydroxy-2-(5-hydroxy-1,4-dioxo-1,4-dihydro-naphthalen-2-yl)-5-methyl-phenyl]-acetamide(200508-07-2)

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: 200508-07-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 200508-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,5,0 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 200508-07:
(8*2)+(7*0)+(6*0)+(5*5)+(4*0)+(3*8)+(2*0)+(1*7)=72
72 % 10 = 2
So 200508-07-2 is a valid CAS Registry Number.

200508-07-2Upstream product

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200508-07-2Relevant academic research and scientific papers

Synthesis of benzo[b]carbazoloquinones by coupling of organostannanes with bromoquinones

Echavarren, Antonio M.,Tamayo, Nuria,De Frutos, Oscar,Garcia, Alicia

, p. 16835 - 16846 (1997)

The synthesis of 5-carbonitrile-1,7-dihydroxy-3-methyl-SH- benzo[b]carbazole-6,11-dione, the quinone originally proposed as prekinamycin, was completed by using a palladium and copper catalyzed Stille reaction as the key step. A subsequent heterocyclizati

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