Cas 1403673-32-4,(R)-2-methyl-6-nitro-1-[N'-p-toluenesulfonyl-(S)-prolyl]-1,2,3,4-tetrahydroquinoline

1403673-32-4

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Basic information

Product Name: (R)-2-methyl-6-nitro-1-[N'-p-toluenesulfonyl-(S)-prolyl]-1,2,3,4-tetrahydroquinoline
Synonyms: (R)-2-methyl-6-nitro-1-[N'-p-toluenesulfonyl-(S)-prolyl]-1,2,3,4-tetrahydroquinoline
CAS NO:1403673-32-4
Molecular Formula:
Molecular Weight: 443.524
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: (R)-2-methyl-6-nitro-1-[N'-p-toluenesulfonyl-(S)-prolyl]-1,2,3,4-tetrahydroquinoline(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-methyl-6-nitro-1-[N'-p-toluenesulfonyl-(S)-prolyl]-1,2,3,4-tetrahydroquinoline(1403673-32-4)
EPA Substance Registry System: (R)-2-methyl-6-nitro-1-[N'-p-toluenesulfonyl-(S)-prolyl]-1,2,3,4-tetrahydroquinoline(1403673-32-4)

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: 1403673-32-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1403673-32-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,6,7 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1403673-32:
(9*1)+(8*4)+(7*0)+(6*3)+(5*6)+(4*7)+(3*3)+(2*3)+(1*2)=134
134 % 10 = 4
So 1403673-32-4 is a valid CAS Registry Number.

1403673-32-4Upstream product

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1403673-32-4Relevant academic research and scientific papers

Synthesis of enantiomers of 6-nitro-and 6-amino-2-methyl-1,2,3,4- tetrahydroquinolines

Gruzdev,Levit,Kodess,Krasnov

, (2012)

Enantiomers of 2-methyl-6-nitro-1,2,3,4-tetrahydroquinoline have been obtained by kinetic resolution of racemic 2-methyl-1,2,3,4-tetrahydroquinoline in acylation with acyl chlorides of N-protected amino acids followed by regioselective nitration of the di

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