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194425-29-1

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194425-29-1 Usage

Chemical structure

Contains a 1,3,4-oxadiazole ring and a 3-acetyl-5-[(4-chlorophenoxy)methyl]-2,3-dihydro-2-phenyl moiety.

Potential applications

Used in the research of pharmaceuticals and agrochemicals.

Biological activities

Has potential biological activities.

Medical applications

May have applications in the development of drugs for various medical conditions.

Chemical properties

Unique chemical structure and potential pharmacological properties.

Synthesis

May be used as a building block in the synthesis of other complex organic compounds.

Further research

Further research and development are needed to fully understand the potential uses and properties of this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 194425-29-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,4,2 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 194425-29:
(8*1)+(7*9)+(6*4)+(5*4)+(4*2)+(3*5)+(2*2)+(1*9)=151
151 % 10 = 1
So 194425-29-1 is a valid CAS Registry Number.

194425-29-1Downstream Products

194425-29-1Relevant articles and documents

Synthesis and evaluation of antibacterial and antifungal activities of some novel 2,5-disubstituted-1,3,4-oxadiazoles

Joshi,Unale,Parkale,Nadagouda,Gadaginamath,Ashalata

, p. 319 - 322 (2013/09/24)

4-Chlorophenoxy acetic acid 2 was prepared by the condensation of phenol with monochloroacetic acid. Compound 2 was refluxed with ethanol in the presence of HCI gas yielding ethyl (4-chlorophenoxy) acetate 3. Compound 3 was refluxed with hydrazine hydrate in ethanol which produced 2-(4-chlorophenoxy) acetohydrazide 4. Compound 5a was synthesized by refluxing 2-(4-chlorophenoxy) acetohydrazide 4 with carbon disulfide and KOH in the presence of ethanol. Compound 5a on condensation with pbenzoquinone yielded 2-({4-[(4-chlorophenoxy) methyl]-1,3-4-oxadiazole-2-yl} sulfanyl) benzene-1,4-diol 5b. Oxadiazoles 6a-d were prepared by reacting substituted phenoxy acetic acids with 2-(4-chlorophenoxy) acetohydrazide 4 in the presence of POCI3. Further Schiff bases were synthesized by the reaction of substituted aldehydes with 2-(4-chlorophenoxy) acetohydrazide 4 in presence of ethanol. These Schiff bases on reaction with acetic anhyd gave the corresponding 3-acetyl-2,3-dihydro 1,3,4-oxadiazoles 7ad. Synthesized compounds were characterized on the basis of spectral and analytical data. All the compounds were screened for antimicrobial activity.

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