Cas 1403685-56-2,(2S,3S,4R)-dimethyl 3-(2-tert-butoxy-2-oxoacetyl)-2-phenyl-4-vinylcyclopentane-1,1-dicarboxylate

1403685-56-2

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Basic information

Product Name: (2S,3S,4R)-dimethyl 3-(2-tert-butoxy-2-oxoacetyl)-2-phenyl-4-vinylcyclopentane-1,1-dicarboxylate
Synonyms: (2S,3S,4R)-dimethyl 3-(2-tert-butoxy-2-oxoacetyl)-2-phenyl-4-vinylcyclopentane-1,1-dicarboxylate
CAS NO:1403685-56-2
Molecular Formula:
Molecular Weight: 416.471
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: (2S,3S,4R)-dimethyl 3-(2-tert-butoxy-2-oxoacetyl)-2-phenyl-4-vinylcyclopentane-1,1-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,4R)-dimethyl 3-(2-tert-butoxy-2-oxoacetyl)-2-phenyl-4-vinylcyclopentane-1,1-dicarboxylate(1403685-56-2)
EPA Substance Registry System: (2S,3S,4R)-dimethyl 3-(2-tert-butoxy-2-oxoacetyl)-2-phenyl-4-vinylcyclopentane-1,1-dicarboxylate(1403685-56-2)

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: 1403685-56-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1403685-56-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,6,8 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1403685-56:
(9*1)+(8*4)+(7*0)+(6*3)+(5*6)+(4*8)+(3*5)+(2*5)+(1*6)=152
152 % 10 = 2
So 1403685-56-2 is a valid CAS Registry Number.

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1403685-56-2Relevant academic research and scientific papers

Palladium-catalyzed asymmetric formal [3+2] cycloaddition of vinyl cyclopropanes and β,γ-unsaturated α-keto esters: An effective route to highly functionalized cyclopentanes

Mei, Liang-Yong,Wei, Yin,Xu, Qin,Shi, Min

, p. 7591 - 7599 (2013/01/15)

Palladium-catalyzed asymmetric formal [3+2] cycloaddition of vinyl cyclopropanes and β,γ-unsaturated α-keto esters proceeded smoothly in the presence of chiral imidazoline-phosphine ligands to give the corresponding highly functionalized cyclopentanes in

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