Cas 87680-33-9,3-Methyl-1-phenyl-1-((2R,7S,11bS)-7-phenyl-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-yl)-urea

87680-33-9

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Basic information

Product Name: 3-Methyl-1-phenyl-1-((2R,7S,11bS)-7-phenyl-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-yl)-urea
Synonyms:
CAS NO:87680-33-9
Molecular Formula:
Molecular Weight: 411.547
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: 3-Methyl-1-phenyl-1-((2R,7S,11bS)-7-phenyl-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-yl)-urea(CAS DataBase Reference)
NIST Chemistry Reference: 3-Methyl-1-phenyl-1-((2R,7S,11bS)-7-phenyl-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-yl)-urea(87680-33-9)
EPA Substance Registry System: 3-Methyl-1-phenyl-1-((2R,7S,11bS)-7-phenyl-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-yl)-urea(87680-33-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 87680-33-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87680-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,8 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87680-33:
(7*8)+(6*7)+(5*6)+(4*8)+(3*0)+(2*3)+(1*3)=169
169 % 10 = 9
So 87680-33-9 is a valid CAS Registry Number.

87680-33-9Upstream product

87680-33-9Downstream Products

87680-33-9Relevant academic research and scientific papers

Dealkylation of a Tertiary Amine Group by an Intramolecular Carbamyl Chloride Functionality

Maryanoff, Bruce E.,Molinari, Albert J.,McComsey, David F.,Maryanoff, Cynthia A.,Wooden, Gary P.,Olofson, R. A.

, p. 5074 - 5080 (2007/10/02)

Compounds containing a 4-anilinopiperidine moiety react with phosgene to afford carbamyl chloride hydrochloride derivatives, which rearrange in the presence of nonnucleophilic amine bases.The rearrangement entails intramolecular acylation by the carbamyl

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