Cas 1338471-91-2,2-[2-(3,4-dimethoxyphenyl)ethyl]-4-nitro-1,2,3,5,6,7-hexahydropyrrolo[1,2-c]pyrimidine

1338471-91-2

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Basic information

Product Name: 2-[2-(3,4-dimethoxyphenyl)ethyl]-4-nitro-1,2,3,5,6,7-hexahydropyrrolo[1,2-c]pyrimidine
Synonyms:
CAS NO:1338471-91-2
Molecular Formula:
Molecular Weight: 333.387
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-[2-(3,4-dimethoxyphenyl)ethyl]-4-nitro-1,2,3,5,6,7-hexahydropyrrolo[1,2-c]pyrimidine(CAS DataBase Reference)
NIST Chemistry Reference: 2-[2-(3,4-dimethoxyphenyl)ethyl]-4-nitro-1,2,3,5,6,7-hexahydropyrrolo[1,2-c]pyrimidine(1338471-91-2)
EPA Substance Registry System: 2-[2-(3,4-dimethoxyphenyl)ethyl]-4-nitro-1,2,3,5,6,7-hexahydropyrrolo[1,2-c]pyrimidine(1338471-91-2)

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: 1338471-91-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1338471-91-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,4,7 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1338471-91:
(9*1)+(8*3)+(7*3)+(6*8)+(5*4)+(4*7)+(3*1)+(2*9)+(1*1)=172
172 % 10 = 2
So 1338471-91-2 is a valid CAS Registry Number.

1338471-91-2Upstream product

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1338471-91-2Relevant academic research and scientific papers

Chemistry of nitroenamines. part 2. synthesis of saturated pyrrolo-pyrimidines and -pyrazines

Scheiber, Pal,Toth, Gabor,Pilipecz, Mihaly V.,Varga, Tamas R.,Nemes, Peter

experimental part, p. 2001 - 2010 (2011/10/08)

New saturated pyrrolo-pyrimidines and pyrrolo-pyrazines were synthesized from 2-nitromethylene-pyrrolidine. Additionally, some simple aminomethylated derivatives of Mannich type were prepared. The nitro compounds were reduced into diastereomeric amines, w

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