Cas 134165-39-2,((3S,4S,5R)-2,3-Diphenyl-5-trifluoromethyl-isoxazolidin-4-yl)-methanol

134165-39-2

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Basic information

Product Name: ((3S,4S,5R)-2,3-Diphenyl-5-trifluoromethyl-isoxazolidin-4-yl)-methanol
Synonyms: ((3S,4S,5R)-2,3-Diphenyl-5-trifluoromethyl-isoxazolidin-4-yl)-methanol
CAS NO:134165-39-2
Molecular Formula:
Molecular Weight: 323.315
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: ((3S,4S,5R)-2,3-Diphenyl-5-trifluoromethyl-isoxazolidin-4-yl)-methanol(CAS DataBase Reference)
NIST Chemistry Reference: ((3S,4S,5R)-2,3-Diphenyl-5-trifluoromethyl-isoxazolidin-4-yl)-methanol(134165-39-2)
EPA Substance Registry System: ((3S,4S,5R)-2,3-Diphenyl-5-trifluoromethyl-isoxazolidin-4-yl)-methanol(134165-39-2)

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: 134165-39-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134165-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,1,6 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 134165-39:
(8*1)+(7*3)+(6*4)+(5*1)+(4*6)+(3*5)+(2*3)+(1*9)=112
112 % 10 = 2
So 134165-39-2 is a valid CAS Registry Number.

134165-39-2Upstream product

134165-39-2Downstream Products

134165-39-2Relevant academic research and scientific papers

Synthesis of Trifluoromethyl-Substituted Isoxazolidines and 4,5-Dihydroisoxazoles by 1,3-Dipolar Cycloadditions

Bravo, Pierfrancesco,Bruche, Luca,Mele, Andrea,Zecchi, Gaetano

, p. 719 - 729 (2007/10/02)

A few representatives of the title heterocycles have been prepared from C,N-diphenylnitrone (1) or arylnitrile oxide (2) and the fluorinated derivatives of ethyl crotonate (3a,b).The regio- and stereochemistry of the cycloadducts were determined by 1H and 19F NMR techniques.

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