Cas 131013-13-3,(1R-2-exo-3-exo)-2-carbomethoxy-8-methyl-8-azabicyclo<3.2.1>octyl 3-N-(4'-nitrophenyl)carbamate

131013-13-3

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Basic information

Product Name: (1R-2-exo-3-exo)-2-carbomethoxy-8-methyl-8-azabicyclo<3.2.1>octyl 3-N-(4'-nitrophenyl)carbamate
Synonyms: (1R-2-exo-3-exo)-2-carbomethoxy-8-methyl-8-azabicyclo<3.2.1>octyl 3-N-(4'-nitrophenyl)carbamate
CAS NO:131013-13-3
Molecular Formula:
Molecular Weight: 363.37
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: (1R-2-exo-3-exo)-2-carbomethoxy-8-methyl-8-azabicyclo<3.2.1>octyl 3-N-(4'-nitrophenyl)carbamate(CAS DataBase Reference)
NIST Chemistry Reference: (1R-2-exo-3-exo)-2-carbomethoxy-8-methyl-8-azabicyclo<3.2.1>octyl 3-N-(4'-nitrophenyl)carbamate(131013-13-3)
EPA Substance Registry System: (1R-2-exo-3-exo)-2-carbomethoxy-8-methyl-8-azabicyclo<3.2.1>octyl 3-N-(4'-nitrophenyl)carbamate(131013-13-3)

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: 131013-13-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 131013-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,0,1 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 131013-13:
(8*1)+(7*3)+(6*1)+(5*0)+(4*1)+(3*3)+(2*1)+(1*3)=53
53 % 10 = 3
So 131013-13-3 is a valid CAS Registry Number.

131013-13-3Upstream product

53-21-4 (-)-cocaine hydrochloride

131013-13-3Downstream Products

131013-14-4 (1R-2-exo-3-exo)-2-carbomethoxy-8-methyl-8-azabicyclo<3.2.1>octyl 3-N-(4'-aminophenyl)carbamate

131013-13-3Relevant academic research and scientific papers

Synthesis of 3-carbamoylecgonine methyl ester analogues as inhibitors of cocaine binding and dopamine uptake

Kline Jr.,Wright,Eshleman,Fox,Eldefrawi

, p. 702 - 705 (1991)

Five (1R-2-exo-3-exo)-3-(N-phenylcarbamoyl)ecgonine methyl ester analogues were synthesized and characterized by 1H and 13C NMR, IR, and thermospray MS. The compounds were synthesized in two or three steps as (-)-stereoisomers from (

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