Cas 811808-01-2,N-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin-15-yl)-3-(benzyloxycarbonylamino)propionamide

811808-01-2

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Basic information

Product Name: N-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin-15-yl)-3-(benzyloxycarbonylamino)propionamide
Synonyms: N-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin-15-yl)-3-(benzyloxycarbonylamino)propionamide
CAS NO:811808-01-2
Molecular Formula:
Molecular Weight: 488.538
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: N-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin-15-yl)-3-(benzyloxycarbonylamino)propionamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin-15-yl)-3-(benzyloxycarbonylamino)propionamide(811808-01-2)
EPA Substance Registry System: N-(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin-15-yl)-3-(benzyloxycarbonylamino)propionamide(811808-01-2)

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: 811808-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 811808-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,1,8,0 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 811808-01:
(8*8)+(7*1)+(6*1)+(5*8)+(4*0)+(3*8)+(2*0)+(1*1)=142
142 % 10 = 2
So 811808-01-2 is a valid CAS Registry Number.

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811808-01-2Relevant academic research and scientific papers

N-methylcarbazole-3-carboxylic acid and its amides

Plekhanova,Ovchinnikov,Glibin

, p. 372 - 376 (2004)

N-Methylcarbazole-3-carboxylic acid was synthesized from N-methyl-2-amino-4-carboxydiphenyl-amine through the corresponding diazo compound by a modified Pschorr procedure. The acid was converted into N-methylcarbazole-3-carbonyl chloride which was treated

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