Cas 1412913-06-4,(3aR,4S,6aS)-ethyl 2-(naphthalen-1ylmethyl)-4-(4-nitrophenyl)-1,3-dioxo-1,2,3,3a,4,6a-hexahydrocyclopenta[c]pyrrole-5-carboxylate

1412913-06-4

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Basic information

Product Name: (3aR,4S,6aS)-ethyl 2-(naphthalen-1ylmethyl)-4-(4-nitrophenyl)-1,3-dioxo-1,2,3,3a,4,6a-hexahydrocyclopenta[c]pyrrole-5-carboxylate
Synonyms: (3aR,4S,6aS)-ethyl 2-(naphthalen-1ylmethyl)-4-(4-nitrophenyl)-1,3-dioxo-1,2,3,3a,4,6a-hexahydrocyclopenta[c]pyrrole-5-carboxylate
CAS NO:1412913-06-4
Molecular Formula:
Molecular Weight: 470.481
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: (3aR,4S,6aS)-ethyl 2-(naphthalen-1ylmethyl)-4-(4-nitrophenyl)-1,3-dioxo-1,2,3,3a,4,6a-hexahydrocyclopenta[c]pyrrole-5-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,4S,6aS)-ethyl 2-(naphthalen-1ylmethyl)-4-(4-nitrophenyl)-1,3-dioxo-1,2,3,3a,4,6a-hexahydrocyclopenta[c]pyrrole-5-carboxylate(1412913-06-4)
EPA Substance Registry System: (3aR,4S,6aS)-ethyl 2-(naphthalen-1ylmethyl)-4-(4-nitrophenyl)-1,3-dioxo-1,2,3,3a,4,6a-hexahydrocyclopenta[c]pyrrole-5-carboxylate(1412913-06-4)

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1412913-06-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1412913-06-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,2,9,1 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1412913-06:
(9*1)+(8*4)+(7*1)+(6*2)+(5*9)+(4*1)+(3*3)+(2*0)+(1*6)=124
124 % 10 = 4
So 1412913-06-4 is a valid CAS Registry Number.

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1412913-06-4Relevant academic research and scientific papers

Chiral multifunctional thiourea-phosphine catalyzed asymmetric [3 + 2] annulation of Morita-Baylis-Hillman carbonates with maleimides

Deng, Hong-Ping,Wang, De,Wei, Yin,Shi, Min

, p. 1098 - 1104 (2012)

We have developed a multifunctional thiourea-phosphine catalyzed asymmetric [3 + 2] annulation of Morita-Baylis-Hillman (MBH) carbonates with maleimides, which can efficiently construct functionalized cyclopentenes bearing three contiguous stereocenters in moderate to excellent yields and excellent diastereo- and enantioselectivities. A plausible mechanism has been also proposed on the basis of control experiments and previous literature.

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