Cas 1100358-79-9,ethyl 3-(4-trifluoromethylphenyl)-4,5-dihydroisoxazole-5-carboxylate

1100358-79-9

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Basic information

Product Name: ethyl 3-(4-trifluoromethylphenyl)-4,5-dihydroisoxazole-5-carboxylate
Synonyms: ethyl 3-(4-trifluoromethylphenyl)-4,5-dihydroisoxazole-5-carboxylate
CAS NO:1100358-79-9
Molecular Formula:
Molecular Weight: 287.238
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: ethyl 3-(4-trifluoromethylphenyl)-4,5-dihydroisoxazole-5-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 3-(4-trifluoromethylphenyl)-4,5-dihydroisoxazole-5-carboxylate(1100358-79-9)
EPA Substance Registry System: ethyl 3-(4-trifluoromethylphenyl)-4,5-dihydroisoxazole-5-carboxylate(1100358-79-9)

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: 1100358-79-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1100358-79-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,0,3,5 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1100358-79:
(9*1)+(8*1)+(7*0)+(6*0)+(5*3)+(4*5)+(3*8)+(2*7)+(1*9)=99
99 % 10 = 9
So 1100358-79-9 is a valid CAS Registry Number.

1100358-79-9Upstream product

1100358-79-9Downstream Products

1100358-79-9Relevant academic research and scientific papers

Enantioselective 1,3-dipolar cycloaddition reactions using chiral lanthanide catalysts

Golebiewski, W. Marek,Gucma, Miroslaw

experimental part, p. 1687 - 1693 (2009/09/06)

(Chemical Equation Presented) Regio- and stereoselective 1,3-dipolar cycloaddition of nitrile oxides to internal 2-pentenols, α,β- unsaturated esters and amides catalyzed by R-(+) BINOL-lanthanide complexes affords corresponding 3-aryl-2-isoxazolines with

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