Cas 372522-66-2,<i>N</i>-benzyl-<i>N</i>-(4-methoxycarbonyloxy-2-triethylsilanyl-but-2-enyl)-malonamic acid methyl ester

372522-66-2

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Basic information

Product Name: N-benzyl-N-(4-methoxycarbonyloxy-2-triethylsilanyl-but-2-enyl)-malonamic acid methyl ester
Synonyms: N-benzyl-N-(4-methoxycarbonyloxy-2-triethylsilanyl-but-2-enyl)-malonamic acid methyl ester
CAS NO:372522-66-2
Molecular Formula:
Molecular Weight: 449.62
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: N-benzyl-N-(4-methoxycarbonyloxy-2-triethylsilanyl-but-2-enyl)-malonamic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: N-benzyl-N-(4-methoxycarbonyloxy-2-triethylsilanyl-but-2-enyl)-malonamic acid methyl ester(372522-66-2)
EPA Substance Registry System: N-benzyl-N-(4-methoxycarbonyloxy-2-triethylsilanyl-but-2-enyl)-malonamic acid methyl ester(372522-66-2)

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: 372522-66-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 372522-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,2,5,2 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 372522-66:
(8*3)+(7*7)+(6*2)+(5*5)+(4*2)+(3*2)+(2*6)+(1*6)=142
142 % 10 = 2
So 372522-66-2 is a valid CAS Registry Number.

372522-66-2Upstream product

372522-66-2Downstream Products

372522-66-2Relevant academic research and scientific papers

Silylated pyrrolidones via diastereoselective Pd-catalysed intramolecular allylic alkylations

Poli, Giovanni,Giambastiani, Giuliano,Malacria, Max,Thorimbert, Serge

, p. 6287 - 6289 (2007/10/03)

A new palladium-catalysed allylic alkylation affording silylated 3-vinyl-pyrrolidones has been developed. The method relies upon the interaction between a stabilised acetamide enolate anion and a silicon-containing nitrogen-tethered η3-allyl-pa

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