Cas 71168-06-4,(3aS,9bR)-1-Phenyl-1,4,5,9b-tetrahydro-naphtho[1,2-d][1,2,3]triazole-3a-carboxylic acid methyl ester

71168-06-4

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Basic information

Product Name: (3aS,9bR)-1-Phenyl-1,4,5,9b-tetrahydro-naphtho[1,2-d][1,2,3]triazole-3a-carboxylic acid methyl ester
Synonyms:
CAS NO:71168-06-4
Molecular Formula:
Molecular Weight: 307.352
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: (3aS,9bR)-1-Phenyl-1,4,5,9b-tetrahydro-naphtho[1,2-d][1,2,3]triazole-3a-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,9bR)-1-Phenyl-1,4,5,9b-tetrahydro-naphtho[1,2-d][1,2,3]triazole-3a-carboxylic acid methyl ester(71168-06-4)
EPA Substance Registry System: (3aS,9bR)-1-Phenyl-1,4,5,9b-tetrahydro-naphtho[1,2-d][1,2,3]triazole-3a-carboxylic acid methyl ester(71168-06-4)

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: 71168-06-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 71168-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,1,6 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71168-06:
(7*7)+(6*1)+(5*1)+(4*6)+(3*8)+(2*0)+(1*6)=114
114 % 10 = 4
So 71168-06-4 is a valid CAS Registry Number.

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71168-06-4Relevant academic research and scientific papers

ETUDE DE LA DIASTEREOSELECTIVITE DE LA CYCLOADDITION DIPOLAIRE-1,3 REACTION DES AZIDES SUR LES METHOXYCARBONYL-3 DIHYDRO-1,2 NAPHTALENES SUBSTITUES ET QUELQUES COMPOSES APPARENTES

Vebrel, Joel,Carrie, Robert

, p. 4163 - 4174 (2007/10/02)

Cycloaddition of azides to 1-or 2-monosubstituted 3-methoxycarbonyl-1,2-dihydro naphtalenes is diastereospecific.The determinant effect revealing a dominant role of conformational factors on the stereochemistry of these reactions.

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