Cas 1004973-32-3,(S,Z)-tert-butyl 2-cyano-5-phenyl-2-(2,2,2-trifluoro-1-(2-nitrophenylimino)ethyl)pentanoate

1004973-32-3

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Basic information

Product Name: (S,Z)-tert-butyl 2-cyano-5-phenyl-2-(2,2,2-trifluoro-1-(2-nitrophenylimino)ethyl)pentanoate
Synonyms:
CAS NO:1004973-32-3
Molecular Formula:
Molecular Weight: 475.467
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: (S,Z)-tert-butyl 2-cyano-5-phenyl-2-(2,2,2-trifluoro-1-(2-nitrophenylimino)ethyl)pentanoate(CAS DataBase Reference)
NIST Chemistry Reference: (S,Z)-tert-butyl 2-cyano-5-phenyl-2-(2,2,2-trifluoro-1-(2-nitrophenylimino)ethyl)pentanoate(1004973-32-3)
EPA Substance Registry System: (S,Z)-tert-butyl 2-cyano-5-phenyl-2-(2,2,2-trifluoro-1-(2-nitrophenylimino)ethyl)pentanoate(1004973-32-3)

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: 1004973-32-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1004973-32-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,4,9,7 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1004973-32:
(9*1)+(8*0)+(7*0)+(6*4)+(5*9)+(4*7)+(3*3)+(2*3)+(1*2)=123
123 % 10 = 3
So 1004973-32-3 is a valid CAS Registry Number.

1004973-32-3Upstream product

1004973-32-3Downstream Products

1004973-32-3Relevant academic research and scientific papers

Enantioselective organocatalytic substitution of α-cyanoacetates on imidoyl chlorides - Synthesis of optically active ketimines

Santoro, Stefano,Poulsen, Thomas B.,Jorgensen, Karl Anker

, p. 5155 - 5157 (2008/09/18)

The enantioselective substitution of α-cyanoacetates on imidoyl chlorides under phase-transfer catalytic conditions is presented; a simple quinidine-derived phase-transfer catalyst gives access to the products, highly substituted ketimines, in generally g

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