Cas 936823-32-4,ethyl 3-(9,10-dioxo-9,10-dihydroanthracen-2-yl)-2-[(4-methylphenyl)sulfonamido]propanoate

936823-32-4

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Basic information

Product Name: ethyl 3-(9,10-dioxo-9,10-dihydroanthracen-2-yl)-2-[(4-methylphenyl)sulfonamido]propanoate
Synonyms: ethyl 3-(9,10-dioxo-9,10-dihydroanthracen-2-yl)-2-[(4-methylphenyl)sulfonamido]propanoate
CAS NO:936823-32-4
Molecular Formula:
Molecular Weight: 477.538
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: ethyl 3-(9,10-dioxo-9,10-dihydroanthracen-2-yl)-2-[(4-methylphenyl)sulfonamido]propanoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 3-(9,10-dioxo-9,10-dihydroanthracen-2-yl)-2-[(4-methylphenyl)sulfonamido]propanoate(936823-32-4)
EPA Substance Registry System: ethyl 3-(9,10-dioxo-9,10-dihydroanthracen-2-yl)-2-[(4-methylphenyl)sulfonamido]propanoate(936823-32-4)

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: 936823-32-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 936823-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,8,2 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 936823-32:
(8*9)+(7*3)+(6*6)+(5*8)+(4*2)+(3*3)+(2*3)+(1*2)=194
194 % 10 = 4
So 936823-32-4 is a valid CAS Registry Number.

936823-32-4Upstream product

936823-32-4Downstream Products

936823-32-4Relevant academic research and scientific papers

Synthesis of novel quinone-amino acid hybrids via cross-enyne metathesis and Diels-Alder reaction as key steps

Kotha, Sambasivarao,Mandal, Kalyaneswar,Banerjee, Shaibal,Mobin, Shaikh M.

, p. 1244 - 1255 (2008/09/17)

A "Building Block Approach" for the synthesis of various quinone-amino acid hybrids through ethylene cross-enyne metathesis and Diels-Alder reaction as key steps is described. A library of comformationally constrained quinone-based phenylalanine derivativ

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