Cas 160154-07-4,3-(3,5-Dichloro-2,4,6-trimethyl-phenyl)-5-fluoromethyl-4-((S)-toluene-4-sulfinyl)-isoxazole

160154-07-4

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Basic information

Product Name: 3-(3,5-Dichloro-2,4,6-trimethyl-phenyl)-5-fluoromethyl-4-((S)-toluene-4-sulfinyl)-isoxazole
Synonyms:
CAS NO:160154-07-4
Molecular Formula:
Molecular Weight: 426.339
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: 3-(3,5-Dichloro-2,4,6-trimethyl-phenyl)-5-fluoromethyl-4-((S)-toluene-4-sulfinyl)-isoxazole(CAS DataBase Reference)
NIST Chemistry Reference: 3-(3,5-Dichloro-2,4,6-trimethyl-phenyl)-5-fluoromethyl-4-((S)-toluene-4-sulfinyl)-isoxazole(160154-07-4)
EPA Substance Registry System: 3-(3,5-Dichloro-2,4,6-trimethyl-phenyl)-5-fluoromethyl-4-((S)-toluene-4-sulfinyl)-isoxazole(160154-07-4)

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: 160154-07-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 160154-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,1,5 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 160154-07:
(8*1)+(7*6)+(6*0)+(5*1)+(4*5)+(3*4)+(2*0)+(1*7)=94
94 % 10 = 4
So 160154-07-4 is a valid CAS Registry Number.

160154-07-4Upstream product

160154-07-4Downstream Products

160154-07-4Relevant academic research and scientific papers

HIGH ASYMMETRIC INDUCTION IN INTERMOLECULAR 1,3-DIPOLAR CYCLOADDITIONS OF NITRILE OXIDES TO CHIRAL VINYL SULPHOXIDES

Bravo, Pierfrancesco,Bruche, Luca,Merli, Annamaria,Fronza, Giovanni

, p. 275 - 278 (2007/10/02)

Asymmetric 1,3-dipolar cycloaddition of nitrile oxides 2 to the chiral methyl enol ether of (R)-3-fluoro-1-(p-tolylsulphinyl)-2-propanone, 3, is described, leading to chiral 4,5-dihydroisoxazoles 4 with high diastereoselectivity.

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