Cas 114156-65-9,(4R,5R)-4-Methyl-3-phenyl-4,5-dihydro-isoxazole-5-carboxylic acid (1R,2S,4R)-1,7,7-trimethyl-2-phenyl-bicyclo[2.2.1]hept-2-yl ester

114156-65-9

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Basic information

Product Name: (4R,5R)-4-Methyl-3-phenyl-4,5-dihydro-isoxazole-5-carboxylic acid (1R,2S,4R)-1,7,7-trimethyl-2-phenyl-bicyclo[2.2.1]hept-2-yl ester
Synonyms:
CAS NO:114156-65-9
Molecular Formula:
Molecular Weight: 417.548
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: (4R,5R)-4-Methyl-3-phenyl-4,5-dihydro-isoxazole-5-carboxylic acid (1R,2S,4R)-1,7,7-trimethyl-2-phenyl-bicyclo[2.2.1]hept-2-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5R)-4-Methyl-3-phenyl-4,5-dihydro-isoxazole-5-carboxylic acid (1R,2S,4R)-1,7,7-trimethyl-2-phenyl-bicyclo[2.2.1]hept-2-yl ester(114156-65-9)
EPA Substance Registry System: (4R,5R)-4-Methyl-3-phenyl-4,5-dihydro-isoxazole-5-carboxylic acid (1R,2S,4R)-1,7,7-trimethyl-2-phenyl-bicyclo[2.2.1]hept-2-yl ester(114156-65-9)

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: 114156-65-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114156-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,5 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114156-65:
(8*1)+(7*1)+(6*4)+(5*1)+(4*5)+(3*6)+(2*6)+(1*5)=99
99 % 10 = 9
So 114156-65-9 is a valid CAS Registry Number.

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114156-65-9Relevant academic research and scientific papers

Asymmetric 1,3-Dipolar Cycloadditions of Nitrile Oxides Using Simple Chiral Auxiliaries

Olsson, Thomas,Stern, Kaye

, p. 2468 - 2472 (1988)

Dipolar cycloadditions of nitrile oxides to substituted bornyl crotonates give substituted isoxazolines with up to 80percent diastereoselectivity.Both regioisomers of the adducts are produced in a ratio of approximately 3:1, independent of the substituent

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