Cas 1616482-53-1,diethyl 4-nitro-3-(3-nitrophenyl)-5-(4-nitrophenyl)pyrrolidine-2,2-dicarboxylate

1616482-53-1

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Basic information

Product Name: diethyl 4-nitro-3-(3-nitrophenyl)-5-(4-nitrophenyl)pyrrolidine-2,2-dicarboxylate
Synonyms: diethyl 4-nitro-3-(3-nitrophenyl)-5-(4-nitrophenyl)pyrrolidine-2,2-dicarboxylate
CAS NO:1616482-53-1
Molecular Formula:
Molecular Weight: 502.437
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: diethyl 4-nitro-3-(3-nitrophenyl)-5-(4-nitrophenyl)pyrrolidine-2,2-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl 4-nitro-3-(3-nitrophenyl)-5-(4-nitrophenyl)pyrrolidine-2,2-dicarboxylate(1616482-53-1)
EPA Substance Registry System: diethyl 4-nitro-3-(3-nitrophenyl)-5-(4-nitrophenyl)pyrrolidine-2,2-dicarboxylate(1616482-53-1)

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: 1616482-53-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1616482-53-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,6,4,8 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1616482-53:
(9*1)+(8*6)+(7*1)+(6*6)+(5*4)+(4*8)+(3*2)+(2*5)+(1*3)=171
171 % 10 = 1
So 1616482-53-1 is a valid CAS Registry Number.

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1616482-53-1Relevant academic research and scientific papers

Chiral phosphoric acid catalyzed 1,3-dipolar cycloadditions of aldehydes, diethyl α-aminomalonate, and nitroalkenes

Luo, Wenqiang,Lin, Yongjun,Yang, Dengshan,He, Long

, p. 787 - 791 (2014)

A one-pot three component 1,3-dipolar cycloaddition reaction of an aldehyde, α-aminomalonate, and nitroalkene has been developed through binaphthol derived chiral phosphoric acids. This reaction represents one of the most enantioselective catalytic approaches to access structurally diverse pyrrolidine derivatives.

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