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349622-01-1

2,2'-[1,4-phenylenedi(carbonyl)]bis(N-phenylhydrazinecarboxamide) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 349622-01-1 Structure

  • Basic information

    1. Product Name: 2,2'-[1,4-phenylenedi(carbonyl)]bis(N-phenylhydrazinecarboxamide)
    2. Synonyms: 2,2'-[1,4-phenylenedi(carbonyl)]bis(N-phenylhydrazinecarboxamide);2,2'-(benzene-1,4-diyldicarbonyl)bis(N-phenylhydrazinecarboxamide)
    3. CAS NO:349622-01-1
    4. Molecular Formula: C22H20N6O4
    5. Molecular Weight: 432.432
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 349622-01-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,2'-[1,4-phenylenedi(carbonyl)]bis(N-phenylhydrazinecarboxamide)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2'-[1,4-phenylenedi(carbonyl)]bis(N-phenylhydrazinecarboxamide)(349622-01-1)
    11. EPA Substance Registry System: 2,2'-[1,4-phenylenedi(carbonyl)]bis(N-phenylhydrazinecarboxamide)(349622-01-1)

  • 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: 349622-01-1(Hazardous Substances Data)

349622-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 349622-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,9,6,2 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 349622-01:
(8*3)+(7*4)+(6*9)+(5*6)+(4*2)+(3*2)+(2*0)+(1*1)=151
151 % 10 = 1
So 349622-01-1 is a valid CAS Registry Number.

349622-01-1Downstream Products

349622-01-1Relevant articles and documents

Synthesis and biological activities of novel 1,4-bridged bis-1,2,4-triazoles, bis-1,3,4-thiadiazoles and bis-1,3,4-oxadiazoles

Shaker,Mahmoud,Abdel-Latif

, p. 397 - 406 (2007/10/03)

The terephthalic acid hydrazide (1) reacted with phenyl / benzyl isothiocyanate 2a,b to yield the corresponding bis-thiosemicarbazides 4a,b, via acid hydrolysis of the intermediate 3 whereas cyclization of 4 gave the bis-1,2,4-triazoles 5,6 and bis-1,3,4-

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