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(3R,5S)-5-(1-Methoxy-vinyl)-5-methyl-2,3-diphenyl-isoxazolidine is a complex organic compound characterized by its unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, with the R and S configurations at the 3rd and 5th carbon atoms, respectively. The compound features a 5-membered isoxazolidine ring, which is fused to two phenyl rings at the 2nd and 3rd carbon atoms. A 1-methoxy-vinyl group is attached to the 5th carbon, and a methyl group is present at the same position, contributing to the molecule's steric properties. This specific arrangement of functional groups and stereochemistry gives rise to distinct physical and chemical properties, making it a potentially valuable compound in various applications, such as pharmaceuticals or materials science, where the precise arrangement of atoms can significantly influence the compound's activity or behavior.

97651-53-1

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97651-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97651-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,6,5 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97651-53:
(7*9)+(6*7)+(5*6)+(4*5)+(3*1)+(2*5)+(1*3)=171
171 % 10 = 1
So 97651-53-1 is a valid CAS Registry Number.

97651-53-1Downstream Products

97651-53-1Relevant academic research and scientific papers

REGIOSELECTIVITY IN THE CYCLOADDITION OF NITRONES TO 2-ALKOXY-1,3-BUTADIENES

Frolkov, A. N.,Kheruze, Yu. I.,Chistokletov, V. N.,Petrov, A. A.

, p. 662 - 665 (2007/10/02)

The cycloaddition of C,N-diphenyl- and C-benzoyl-N-phenylnitrones to 2-Alkoxy-1,3-alkadienes leads to 5-substituted isoxazolidines.Irrespective of the substituent at the C atom of the nitrone, the structure of the alkoxyl radical of the dipolarophile, and the reaction conditions, the addition of the nitrones to 2-substituted dienyl ethers only takes place at the unsubstituted double bond.In the case of 2-isopropoxy- and 2-tert-butoxy-1,3-butadienes a mixture of diastereomers is formed.

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