Cas 1053231-50-7,(3R,3aR,6aR)-3-[(S)-2-(benzoxy)benzyl]-2-benzyl-4,5-oxathiain-4,4-dioxide[3,4-d]isoxazolidine

1053231-50-7

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Basic information

Product Name: (3R,3aR,6aR)-3-[(S)-2-(benzoxy)benzyl]-2-benzyl-4,5-oxathiain-4,4-dioxide[3,4-d]isoxazolidine
Synonyms:
CAS NO:1053231-50-7
Molecular Formula:
Molecular Weight: 451.543
EINECS: N/A
Product Categories: N/A
Mol File: 1053231-50-7.mol
Article Data: 1

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: (3R,3aR,6aR)-3-[(S)-2-(benzoxy)benzyl]-2-benzyl-4,5-oxathiain-4,4-dioxide[3,4-d]isoxazolidine(CAS DataBase Reference)
NIST Chemistry Reference: (3R,3aR,6aR)-3-[(S)-2-(benzoxy)benzyl]-2-benzyl-4,5-oxathiain-4,4-dioxide[3,4-d]isoxazolidine(1053231-50-7)
EPA Substance Registry System: (3R,3aR,6aR)-3-[(S)-2-(benzoxy)benzyl]-2-benzyl-4,5-oxathiain-4,4-dioxide[3,4-d]isoxazolidine(1053231-50-7)

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: 1053231-50-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1053231-50-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,3,2,3 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1053231-50:
(9*1)+(8*0)+(7*5)+(6*3)+(5*2)+(4*3)+(3*1)+(2*5)+(1*0)=97
97 % 10 = 7
So 1053231-50-7 is a valid CAS Registry Number.

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1053231-50-7Relevant articles and documents

Regio- and stereoselective synthesis of isoxazolidine derivatives by asymmetric 1,3-dipolar cycloaddition reaction of chiral nitrones with 1-propene-1,3-sultone

Zhang, Hong-Kui,Chan, Wing-Hong,Lee, Albert W. M.,Wong, Wai-Yeung

, p. 957 - 962 (2008/12/20)

(Chemical Equation Presented) Asymmetric 1,3-dipolar cycloadditions of chiral nitrones to 1-propene-1,3-sultone (1) were investigated. Chiral nitrones 6a-e reacted with sultone 1 in toluene at 90°C for 24-36 h to give the corresponding isoxazolidines in m

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