Cas 810690-63-2,4-methyl-N-[3-(4-nitro-benzenesulfonyl)-allyl]-N-(2-oxo-ethyl)-benzenesulfonamide

810690-63-2

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Basic information

Product Name: 4-methyl-N-[3-(4-nitro-benzenesulfonyl)-allyl]-N-(2-oxo-ethyl)-benzenesulfonamide
Synonyms: 4-methyl-N-[3-(4-nitro-benzenesulfonyl)-allyl]-N-(2-oxo-ethyl)-benzenesulfonamide
CAS NO:810690-63-2
Molecular Formula:
Molecular Weight: 438.482
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: 4-methyl-N-[3-(4-nitro-benzenesulfonyl)-allyl]-N-(2-oxo-ethyl)-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-methyl-N-[3-(4-nitro-benzenesulfonyl)-allyl]-N-(2-oxo-ethyl)-benzenesulfonamide(810690-63-2)
EPA Substance Registry System: 4-methyl-N-[3-(4-nitro-benzenesulfonyl)-allyl]-N-(2-oxo-ethyl)-benzenesulfonamide(810690-63-2)

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: 810690-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 810690-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,0,6,9 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 810690-63:
(8*8)+(7*1)+(6*0)+(5*6)+(4*9)+(3*0)+(2*6)+(1*3)=152
152 % 10 = 2
So 810690-63-2 is a valid CAS Registry Number.

810690-63-2Upstream product

810690-75-6 N-(2,2-diethoxy-ethyl)-4-methyl-N-[3-(4-nitro-benzenesulfonyl)-allyl]-benzenesulfonamide

810690-63-2Downstream Products

810690-68-7 4-{[3-(4-nitro-benzenesulfonyl)-allyl]-(toluene-4-sulfonyl)-amino}-but-2-enethioic acid S-ethyl ester

810690-63-2Relevant academic research and scientific papers

Nucleophilic catalysis via phosphine conjugate addition: Vinyl sulfones as reacting partners in catalytic cross-Michael cycloisomerization

Luis, Ana Liza,Krische, Michael J.

, p. 2579 - 2585 (2007/10/03)

Vinylsulfones serve as highly effective reacting partners in tributylphosphine catalyzed cross-Michael cycloisomerization. In all cases examined, the vinylsulfone moiety exclusively serves as the Michael acceptor to provide 5- and 6-membered ring products

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