Cas 118304-02-2,(3aS,5R,9bS)-5-Phenyl-1,4,5,9b-tetrahydro-benzo[e]indazole-3a-carboxylic acid methyl ester

118304-02-2

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Basic information

Product Name: (3aS,5R,9bS)-5-Phenyl-1,4,5,9b-tetrahydro-benzo[e]indazole-3a-carboxylic acid methyl ester
Synonyms: (3aS,5R,9bS)-5-Phenyl-1,4,5,9b-tetrahydro-benzo[e]indazole-3a-carboxylic acid methyl ester
CAS NO:118304-02-2
Molecular Formula:
Molecular Weight: 306.364
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,5R,9bS)-5-Phenyl-1,4,5,9b-tetrahydro-benzo[e]indazole-3a-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,5R,9bS)-5-Phenyl-1,4,5,9b-tetrahydro-benzo[e]indazole-3a-carboxylic acid methyl ester(118304-02-2)
EPA Substance Registry System: (3aS,5R,9bS)-5-Phenyl-1,4,5,9b-tetrahydro-benzo[e]indazole-3a-carboxylic acid methyl ester(118304-02-2)

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: 118304-02-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 118304-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,0 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 118304-02:
(8*1)+(7*1)+(6*8)+(5*3)+(4*0)+(3*4)+(2*0)+(1*2)=92
92 % 10 = 2
So 118304-02-2 is a valid CAS Registry Number.

118304-02-2Upstream product

118304-02-2Downstream Products

118304-09-9 (3aS,5R,9bR)-5-Phenyl-3,4,5,9b-tetrahydro-benzo[e]indazole-3a-carboxylic acid methyl ester

118304-02-2Relevant academic research and scientific papers

Study on the diastereospecificity of diazomethane cycloadditions to substituted 1,2-dihydro naphthalenes

Vebrel, Joel,Tonnard, Francois,Carrie, Robert

, p. 1056 - 1064 (2007/10/02)

The 1,2-dihydro-3-carbomethoxynaphthalenes substituted at the 1 or 2 position by alkyl groups add diazomethane diastereospecifically to give adducts in which the substituent is cis to the ester group.This establishes the importance of conformational facto

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