Cas 1189113-54-9,2-(((4,5-dihydro-3-(4-methoxyphenyl)isoxazol-5-yl)methoxy)methyl)-5-p-tolyl-1,3,4-oxadiazole

1189113-54-9

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Basic information

Product Name: 2-(((4,5-dihydro-3-(4-methoxyphenyl)isoxazol-5-yl)methoxy)methyl)-5-p-tolyl-1,3,4-oxadiazole
Synonyms:
CAS NO:1189113-54-9
Molecular Formula:
Molecular Weight: 379.415
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: 2-(((4,5-dihydro-3-(4-methoxyphenyl)isoxazol-5-yl)methoxy)methyl)-5-p-tolyl-1,3,4-oxadiazole(CAS DataBase Reference)
NIST Chemistry Reference: 2-(((4,5-dihydro-3-(4-methoxyphenyl)isoxazol-5-yl)methoxy)methyl)-5-p-tolyl-1,3,4-oxadiazole(1189113-54-9)
EPA Substance Registry System: 2-(((4,5-dihydro-3-(4-methoxyphenyl)isoxazol-5-yl)methoxy)methyl)-5-p-tolyl-1,3,4-oxadiazole(1189113-54-9)

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: 1189113-54-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1189113-54-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,9,1,1 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1189113-54:
(9*1)+(8*1)+(7*8)+(6*9)+(5*1)+(4*1)+(3*3)+(2*5)+(1*4)=159
159 % 10 = 9
So 1189113-54-9 is a valid CAS Registry Number.

1189113-54-9Upstream product

1189113-85-6 C₂₁H₂₃N₃O₄

1189113-54-9Downstream Products

1189113-54-9Relevant academic research and scientific papers

Synthesis and pharmacological evaluation of 1,3,4-oxadiazole bearing bis(heterocycle) derivatives as anti-inflammatory and analgesic agents

Jayashankar,Lokanath Rai,Baskaran,Sathish

experimental part, p. 3898 - 3902 (2009/12/09)

A series of novel ether-linked bis(heterocycle)s have been synthesized via [3 + 2]-cycloaddition reaction of nitrile oxide with allyl alcohol followed by intramolecular 1,3-diploar cycloaddition reaction of nitrile imine with carbonyl group. All the newly

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