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CAS

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199339-03-2

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

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  • 199339-03-2 Structure

  • Basic information

    1. Product Name: 2-Bromo-N-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionamide
    2. Synonyms:
    3. CAS NO:199339-03-2
    4. Molecular Formula:
    5. Molecular Weight: 296.123
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 199339-03-2.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-Bromo-N-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Bromo-N-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionamide(199339-03-2)
    11. EPA Substance Registry System: 2-Bromo-N-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionamide(199339-03-2)

  • 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: 199339-03-2(Hazardous Substances Data)

199339-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199339-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,3,3 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 199339-03:
(8*1)+(7*9)+(6*9)+(5*3)+(4*3)+(3*9)+(2*0)+(1*3)=182
182 % 10 = 2
So 199339-03-2 is a valid CAS Registry Number.

199339-03-2Relevant articles and documents

Synthesis and antimicrobial activity of some 5-aryl-2-[(N,N-disubstituted thiocarbamoylthio)acylamino]-1,3,4-oxadiazoles

Ates, Oeznur,Kocabalkanli, Ayse,Cesur, Nesrin,Oetuek, Guelten

, p. 541 - 544 (2007/10/03)

In this study, a number of novel 5-aryl-2-[(N,N-disubstituted thiocarbamoylthio)acylamino]-1,3,4-oxadiazole derivatives were synthesized by the reaction of potassium salts of N,N-disubstituted dithiocarbamoic acids with 2-[(α-chloro-α-phenylacetyl/α-bromo

Synthesis and antibacterial activity of 5-aryl-2- [(α-chloro-α-phenylacetyl/α- bromopropionyl)amino]-1,3,4-oxadiazoles and 2-[(5-aryl-1 ,3,4-oxadiazol-2-yl)imino]-5-phenyl/methyl-4-thiazolidinones

Ates, Oeznur,Kocabalkanlr, Ayse,Sanis, Guelten Oetuek,Ekinci, Ahmet C.,Vidin, Aylin

, p. 1134 - 1138 (2007/10/03)

Reaction of 5-aryl-2-amino-1,3,4-oxadiazoles (B(I-VI)), obtained by the oxydative cyclization of aromatic aldehyde semicarbazones (A(I-VI)), with α-chloro-α-phenylacetyl chloride and a-bromopropionyl bromide yielded 5-aryl-2-[(α-chloro-α-phenylacetyl)amino]-1,3,4-oxadiazoles (Ia-VIa) and 5-aryl-2-[(α-bromopropionyl)amino]-1, 3,4-oxadiazoles (VIIa-XIIa), respectively. Furthermore, Ia-XIIa were refluxed with ammonium thiocyanate to give 5-phenyl/methyl-2-[(5-aryl-1,3,4-oxadiazol-2-yl)imino]-4-thiazolidinones (It-XIIt). All compounds were tested for antibacterial activity against Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae and Pseudomonas aeruginosa. They were all found to possess significant activity against S. aureus with MIC values ranging from 0.24 to 125 μg/ml. LD50 of compounds chosen as prototypes are estimated.

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