Cas 1014106-66-1,2-(4-chlorophenyl)-5-(5-methyl-3-(pyridin-3-yl)-4,5-dihydroisoxazol-5-yl)-1,3,4-oxadiazole

1014106-66-1

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Basic information

Product Name: 2-(4-chlorophenyl)-5-(5-methyl-3-(pyridin-3-yl)-4,5-dihydroisoxazol-5-yl)-1,3,4-oxadiazole
Synonyms: 2-(4-chlorophenyl)-5-(5-methyl-3-(pyridin-3-yl)-4,5-dihydroisoxazol-5-yl)-1,3,4-oxadiazole
CAS NO:1014106-66-1
Molecular Formula:
Molecular Weight: 340.769
EINECS: N/A
Product Categories: N/A
Mol File: 1014106-66-1.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: 2-(4-chlorophenyl)-5-(5-methyl-3-(pyridin-3-yl)-4,5-dihydroisoxazol-5-yl)-1,3,4-oxadiazole(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-chlorophenyl)-5-(5-methyl-3-(pyridin-3-yl)-4,5-dihydroisoxazol-5-yl)-1,3,4-oxadiazole(1014106-66-1)
EPA Substance Registry System: 2-(4-chlorophenyl)-5-(5-methyl-3-(pyridin-3-yl)-4,5-dihydroisoxazol-5-yl)-1,3,4-oxadiazole(1014106-66-1)

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: 1014106-66-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1014106-66-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,4,1,0 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1014106-66:
(9*1)+(8*0)+(7*1)+(6*4)+(5*1)+(4*0)+(3*6)+(2*6)+(1*6)=81
81 % 10 = 1
So 1014106-66-1 is a valid CAS Registry Number.

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1014106-66-1Relevant articles and documents

Synthesis and biological activity of 2-(4,5-dihydroisoxazol-5-yl)-1,3,4-oxadiazoles

Milinkevich, Kristin A.,Yoo, Choong L.,Sparks, Thomas C.,Lorsbach, Beth A.,Kurth, Mark J.

supporting information; experimental part, p. 5796 - 5798 (2010/04/30)

Acid hydrazides were coupled with acrylic acid derivatives and cyclodehydration gave 1,3,4-oxadiazoles. Lastly, in-situ nitrile oxide formation from aryl oximes treated with sodium hypochlorite, and subsequent 1,3-dipolar cycloaddition to the exomethylene

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