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2-(phenylsulfonylmethyl)-5-(2-chlorophenyl)-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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  • 1155195-94-0 Structure
  • Basic information

    1. Product Name: 2-(phenylsulfonylmethyl)-5-(2-chlorophenyl)-1,3,4-oxadiazole
    2. Synonyms:
    3. CAS NO:1155195-94-0
    4. Molecular Formula:
    5. Molecular Weight: 334.783
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1155195-94-0.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-(phenylsulfonylmethyl)-5-(2-chlorophenyl)-1,3,4-oxadiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(phenylsulfonylmethyl)-5-(2-chlorophenyl)-1,3,4-oxadiazole(1155195-94-0)
    11. EPA Substance Registry System: 2-(phenylsulfonylmethyl)-5-(2-chlorophenyl)-1,3,4-oxadiazole(1155195-94-0)
  • 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: 1155195-94-0(Hazardous Substances Data)

1155195-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1155195-94-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,5,1,9 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1155195-94:
(9*1)+(8*1)+(7*5)+(6*5)+(5*1)+(4*9)+(3*5)+(2*9)+(1*4)=160
160 % 10 = 0
So 1155195-94-0 is a valid CAS Registry Number.

1155195-94-0Relevant articles and documents

Synthesis, antimicrobial and cytotoxic activities of 1,3,4-oxadiazoles, 1,3,4-thiadiazoles and 1,2,4-triazoles

Padmavathi,Sudhakar Reddy,Padmaja,Kondaiah,Ali-Shazia

, p. 2106 - 2112 (2009)

A new class of 1,3,4-oxadiazoles were prepared from acid hydrazides on treatment with different carboxylic acids in the presence of phosphorus oxychloride. Interconversion of oxadiazoles to thiadiazoles and triazoles was carried out with appropriate reagents. The antimicrobial and cytotoxic activities of compounds 7a-d to 12a-d were tested. Compounds 10d and 12d showed pronounced antimicrobial activity. Further, compound 10d exhibited maximum cytotoxicity.

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