Cas 476437-70-4,2-((S)-3-Oxo-cyclopentyl)-2-(3-oxo-propyl)-malonic acid dibenzyl ester

476437-70-4

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Basic information

Product Name: 2-((S)-3-Oxo-cyclopentyl)-2-(3-oxo-propyl)-malonic acid dibenzyl ester
Synonyms: 2-((S)-3-Oxo-cyclopentyl)-2-(3-oxo-propyl)-malonic acid dibenzyl ester
CAS NO:476437-70-4
Molecular Formula:
Molecular Weight: 422.478
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-((S)-3-Oxo-cyclopentyl)-2-(3-oxo-propyl)-malonic acid dibenzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-((S)-3-Oxo-cyclopentyl)-2-(3-oxo-propyl)-malonic acid dibenzyl ester(476437-70-4)
EPA Substance Registry System: 2-((S)-3-Oxo-cyclopentyl)-2-(3-oxo-propyl)-malonic acid dibenzyl ester(476437-70-4)

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: 476437-70-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 476437-70-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,6,4,3 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 476437-70:
(8*4)+(7*7)+(6*6)+(5*4)+(4*3)+(3*7)+(2*7)+(1*0)=184
184 % 10 = 4
So 476437-70-4 is a valid CAS Registry Number.

476437-70-4Upstream product

476437-70-4Downstream Products

476437-70-4Relevant academic research and scientific papers

Highly enantioselective catalytic Michael reaction of α-substituted malonates using La-linked-BINOL complex in the presence of HFIP (1,1,1,3,3,3-hexafluoroisopropanol)

Takita, Ryo,Ohshima, Takashi,Shibasaki, Masakatsu

, p. 4661 - 4665 (2002)

A catalytic asymmetric Michael reaction of α-substituted malonates with broad generality was developed using the La-linked-BINOL complex. To enhance the reactivity of unreactive α-substituted malonates, we examined the effects of concentration and additiv

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