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2,5-bis((4-chlorophenoxy)methyl)-1,3,4-oxadiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 944529-23-1 Structure
  • Basic information

    1. Product Name: 2,5-bis((4-chlorophenoxy)methyl)-1,3,4-oxadiazole
    2. Synonyms: 2,5-bis((4-chlorophenoxy)methyl)-1,3,4-oxadiazole
    3. CAS NO:944529-23-1
    4. Molecular Formula:
    5. Molecular Weight: 351.189
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 944529-23-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,5-bis((4-chlorophenoxy)methyl)-1,3,4-oxadiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,5-bis((4-chlorophenoxy)methyl)-1,3,4-oxadiazole(944529-23-1)
    11. EPA Substance Registry System: 2,5-bis((4-chlorophenoxy)methyl)-1,3,4-oxadiazole(944529-23-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 944529-23-1(Hazardous Substances Data)

944529-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 944529-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,5,2 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 944529-23:
(8*9)+(7*4)+(6*4)+(5*5)+(4*2)+(3*9)+(2*2)+(1*3)=191
191 % 10 = 1
So 944529-23-1 is a valid CAS Registry Number.

944529-23-1Downstream Products

944529-23-1Relevant 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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