Cas 114247-31-3,(4S,5S)-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

114247-31-3

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Basic information

Product Name: (4S,5S)-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:114247-31-3
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: (4S,5S)-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: (4S,5S)-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(114247-31-3)
EPA Substance Registry System: (4S,5S)-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(114247-31-3)

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: 114247-31-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114247-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,2,4 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 114247-31:
(8*1)+(7*1)+(6*4)+(5*2)+(4*4)+(3*7)+(2*3)+(1*1)=93
93 % 10 = 3
So 114247-31-3 is a valid CAS Registry Number.

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114247-31-3Relevant academic research and scientific papers

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

Olsson, Thomas,Stern, Kaye

, p. 2468 - 2472 (2007/10/02)

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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