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CAS

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64822-04-4

Methanone, phenyl[5-(phenylamino)-1,2,4-thiadiazol-3-yl]-, oxime, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 64822-04-4 Structure

  • Basic information

    1. Product Name: Methanone, phenyl[5-(phenylamino)-1,2,4-thiadiazol-3-yl]-, oxime, (E)-
    2. Synonyms:
    3. CAS NO:64822-04-4
    4. Molecular Formula: C15H12N4OS
    5. Molecular Weight: 296.352
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 64822-04-4.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: Methanone, phenyl[5-(phenylamino)-1,2,4-thiadiazol-3-yl]-, oxime, (E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methanone, phenyl[5-(phenylamino)-1,2,4-thiadiazol-3-yl]-, oxime, (E)-(64822-04-4)
    11. EPA Substance Registry System: Methanone, phenyl[5-(phenylamino)-1,2,4-thiadiazol-3-yl]-, oxime, (E)-(64822-04-4)

  • 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: 64822-04-4(Hazardous Substances Data)

64822-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64822-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,2 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64822-04:
(7*6)+(6*4)+(5*8)+(4*2)+(3*2)+(2*0)+(1*4)=124
124 % 10 = 4
So 64822-04-4 is a valid CAS Registry Number.

64822-04-4Relevant articles and documents

Mononuclear heterocyclic rearrangements. Part 11. Rearrangements of 1,2,4-oxadiazoles, isoxazoles, and 1,2,5-oxadiazoles involving a sulphur atom

Vivona, Nicolo,Cusmano, Giuseppe,Macaluso, Gabriella

, p. 1616 - 1619 (2007/10/04)

The reactions of 3-amino-5-methyl- and 3-amino-5-phenyl-1,2,4-oxadiazoles, 3-amino-5-methylisoxazole, and 3-amino-4-methyl- and 3-amino-4-phenyl-1,2,5- oxadiazoles with phenyl isothiocyanate have been investigated, and the reactivity of phenylthioureido-derivatives (3) of these ring systems towards rearrangement have been studied. The presence of a sulphur atom in the side-chain sequence (1; XYZ = NCS) greatly enhances the reactivity of the systems under consideration towards rearrangement. The tendency of the three heterocycles to rearrange decreases in the order 1,2,4-oxadiazole > isoxazole > 1,2,5-oxadiazole.

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