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4-[3-acetyl-5-(pyridine-4-yl)-2,3-dihydro-1,3,4-oxadiazol-2-yl]phenyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1430799-99-7 Structure
  • Basic information

    1. Product Name: 4-[3-acetyl-5-(pyridine-4-yl)-2,3-dihydro-1,3,4-oxadiazol-2-yl]phenyl acetate
    2. Synonyms:
    3. CAS NO:1430799-99-7
    4. Molecular Formula:
    5. Molecular Weight: 325.324
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1430799-99-7.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: 4-[3-acetyl-5-(pyridine-4-yl)-2,3-dihydro-1,3,4-oxadiazol-2-yl]phenyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[3-acetyl-5-(pyridine-4-yl)-2,3-dihydro-1,3,4-oxadiazol-2-yl]phenyl acetate(1430799-99-7)
    11. EPA Substance Registry System: 4-[3-acetyl-5-(pyridine-4-yl)-2,3-dihydro-1,3,4-oxadiazol-2-yl]phenyl acetate(1430799-99-7)
  • 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: 1430799-99-7(Hazardous Substances Data)

1430799-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1430799-99-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,0,7,9 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1430799-99:
(9*1)+(8*4)+(7*3)+(6*0)+(5*7)+(4*9)+(3*9)+(2*9)+(1*9)=187
187 % 10 = 7
So 1430799-99-7 is a valid CAS Registry Number.

1430799-99-7Downstream Products

1430799-99-7Relevant articles and documents

Endothelium dependent and independent mechanisms of vasorelaxant activity of synthesized 2,5-disubstituted-1,3,4-oxadiazole derivatives in rat thoracic aorta-ex vivo and molecular docking studies

Attari, Zenab,Mudgal, Jayesh,Nayak, Pawan G.,Krishnadas, Nandakumar,Rajappan, Revathi,Gopalan Kutty

, p. 441 - 450 (2016)

Background: Vasoconstriction is a major pathological feature of cardiovascular diseases involving endothelium dependent and independent mechanisms. Oxadiazole moiety appeared to be effective in various pathologies. Objective: The aim of the study was to s

Synthesis and testing of 3-acetyl-2,5-disubstituted-2,3-dihydro-1,3,4- oxadiazole derivatives for antifungal activity against selected Candida species

De Oliveira, Cledualdo S.,Lira, Bruno F.,Barbosa-Filho, Jose? M.,Lorenzo, Jorge G. F.,De Menezes, Camilla P.,Dos Santos, Jessyca M. C. G.,De Lima, Edeltrudes O.,De Athayde-Filho, Petro?nio F.

, p. 115 - 120 (2013/04/24)

A series of 21 1,3,4-oxadiazoline derivatives was synthesized by cyclization of N-acylhydrazones with acetic anhydride and evaluated for their in vitro antifungal activity against six Candida strains: Candida albicans (ATCC 90028 and LM V-42), C. krusei (ATCC 6258 and LM 12 C) and C. tropicalis (ATCC 13803 and LM 14). The Candida strains were found to be sensitive to some of the compounds, which inhibited the growth by 50-90percent, with minimum inhibitory concentration (MIC) in the range of 64-512 μg mL-1. The compounds' structures were fully confirmed and characterized by Fourier transform infrared spectroscopy (FTIR), 1H and 13C nuclear magnetic resonance (NMR) and mass spectrometry (MS).

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