Cas 454711-20-7,1-benzyl-3-(tert.-butyloxycarbonylamino)-4-methyl-piperidine

454711-20-7

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Basic information

Product Name: 1-benzyl-3-(tert.-butyloxycarbonylamino)-4-methyl-piperidine
Synonyms: 1-benzyl-3-(tert.-butyloxycarbonylamino)-4-methyl-piperidine
CAS NO:454711-20-7
Molecular Formula:
Molecular Weight: 304.433
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: 1-benzyl-3-(tert.-butyloxycarbonylamino)-4-methyl-piperidine(CAS DataBase Reference)
NIST Chemistry Reference: 1-benzyl-3-(tert.-butyloxycarbonylamino)-4-methyl-piperidine(454711-20-7)
EPA Substance Registry System: 1-benzyl-3-(tert.-butyloxycarbonylamino)-4-methyl-piperidine(454711-20-7)

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: 454711-20-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 454711-20-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,4,7,1 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 454711-20:
(8*4)+(7*5)+(6*4)+(5*7)+(4*1)+(3*1)+(2*2)+(1*0)=137
137 % 10 = 7
So 454711-20-7 is a valid CAS Registry Number.

454711-20-7Upstream product

454711-21-8 1-benzyl-3-[(tert-butoxycarbonyl)amino]-4-methylpyridinium bromide

454711-20-7Downstream Products

454711-20-7Relevant academic research and scientific papers

Xanthine derivatives, the preparation thereof and their use as pharmaceutical compositions

-

, (2008/06/13)

The present invention relates to substituted xanthines of general formula wherein R1 to R4 are defined as in claim 1, the tautomers and the stereoisomers thereof, mixtures thereof, the prodrugs and the salts thereof which have valuable pharmacological properties, particularly an inhibiting effect on the activity of the enzyme dipeptidylpeptidase-IV (DPP-IV).

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