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CAS

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127722-65-0

2-phenyl-2-<(2-tetrahydropyranyloxy)-2-ethyl> malondiamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127722-65-0 Structure

  • Basic information

    1. Product Name: 2-phenyl-2-<(2-tetrahydropyranyloxy)-2-ethyl> malondiamide
    2. Synonyms:
    3. CAS NO:127722-65-0
    4. Molecular Formula:
    5. Molecular Weight: 306.362
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127722-65-0.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-phenyl-2-<(2-tetrahydropyranyloxy)-2-ethyl> malondiamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-phenyl-2-<(2-tetrahydropyranyloxy)-2-ethyl> malondiamide(127722-65-0)
    11. EPA Substance Registry System: 2-phenyl-2-<(2-tetrahydropyranyloxy)-2-ethyl> malondiamide(127722-65-0)

  • 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: 127722-65-0(Hazardous Substances Data)

127722-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127722-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,2 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127722-65:
(8*1)+(7*2)+(6*7)+(5*7)+(4*2)+(3*2)+(2*6)+(1*5)=130
130 % 10 = 0
So 127722-65-0 is a valid CAS Registry Number.

127722-65-0Downstream Products

127722-65-0Relevant articles and documents

New chemical aspects of primidone metabolism

Lafont,Cave,Menager,Miocque

, p. 61 - 66 (1990)

Primidone is metabolized either into phenylethylmalondiamide or phenobarbital. 2-Hydroxyprimidone was synthesized and tested as a potential intermediate common to these two biodegradation pathways in dogs as well as in vitro. On the other hand, the mechanism of the formation of α-phenyl-γ-butyrolactone during intoxication was investigated and the role of precursor played by the phenobarbital generated in vivo was shown.

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