Cas 1092576-40-3,(2S,3S)-ethyl 3-(naphthalen-1-yl)-4-nitro-2-phenyl-2,3-dihydro-1H-pyrrole-2-carboxylate

1092576-40-3

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Basic information

Product Name: (2S,3S)-ethyl 3-(naphthalen-1-yl)-4-nitro-2-phenyl-2,3-dihydro-1H-pyrrole-2-carboxylate
Synonyms: (2S,3S)-ethyl 3-(naphthalen-1-yl)-4-nitro-2-phenyl-2,3-dihydro-1H-pyrrole-2-carboxylate
CAS NO:1092576-40-3
Molecular Formula:
Molecular Weight: 388.423
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)-ethyl 3-(naphthalen-1-yl)-4-nitro-2-phenyl-2,3-dihydro-1H-pyrrole-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-ethyl 3-(naphthalen-1-yl)-4-nitro-2-phenyl-2,3-dihydro-1H-pyrrole-2-carboxylate(1092576-40-3)
EPA Substance Registry System: (2S,3S)-ethyl 3-(naphthalen-1-yl)-4-nitro-2-phenyl-2,3-dihydro-1H-pyrrole-2-carboxylate(1092576-40-3)

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: 1092576-40-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1092576-40-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,5,7 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1092576-40:
(9*1)+(8*0)+(7*9)+(6*2)+(5*5)+(4*7)+(3*6)+(2*4)+(1*0)=163
163 % 10 = 3
So 1092576-40-3 is a valid CAS Registry Number.

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1092576-40-3Relevant academic research and scientific papers

Organocatalytic asymmetric formal [3+2] cycloaddition reaction of isocyanoesters to nitroolefins leading to highly optically active dihydropyrroles

Guo, Chang,Xue, Meng-Xia,Zhu, Ming-Kui,Gong, Liu-Zhu

, p. 3414 - 3417 (2008)

(Chemical Equation Presented) Closing the circle: The asymmetric [3+2] formal cycloaddition reaction of α-substituted isocyanoesters with nitroolefins is catalyzed by cinchona alkaloid derivatives to yield 2,3-dihydropyrroles with high diastereo- and enan

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