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53567-09-2

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

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  • 53567-09-2 Structure

  • Basic information

    1. Product Name: N-(5-Phenyl-[1,3,4]thiadiazol-2-yl)-formamide
    2. Synonyms: N-(5-Phenyl-[1,3,4]thiadiazol-2-yl)-formamide
    3. CAS NO:53567-09-2
    4. Molecular Formula:
    5. Molecular Weight: 205.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53567-09-2.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: N-(5-Phenyl-[1,3,4]thiadiazol-2-yl)-formamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(5-Phenyl-[1,3,4]thiadiazol-2-yl)-formamide(53567-09-2)
    11. EPA Substance Registry System: N-(5-Phenyl-[1,3,4]thiadiazol-2-yl)-formamide(53567-09-2)

  • 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: 53567-09-2(Hazardous Substances Data)

53567-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53567-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,6 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53567-09:
(7*5)+(6*3)+(5*5)+(4*6)+(3*7)+(2*0)+(1*9)=132
132 % 10 = 2
So 53567-09-2 is a valid CAS Registry Number.

53567-09-2Downstream Products

53567-09-2Relevant articles and documents

Synthesis of 2-(N-formyl)-5-aryl/aryloxymethyl-1,3,4-thiadiazoles with potential bioactivity in PEG-400

Wang, Xi Cun,Ding, Xiao Mei,Wang, Sheng Qing,Chen, Xue Fei,Quan, Zheng Jun

experimental part, p. 301 - 304 (2010/12/19)

An environmental benign procedure for synthesis of 2-(N-formyl)-5-aryl/aryloxymethyl-1,3,4-thiadiazoles has been developed by reaction of 2-amino-5-aryl/aryloxymethyl-1,3,4-thiadiazoles with formic acid in PEG-400. The key advantages of this protocol are

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