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N1,N3-di<(adamantyl-1)-2 oxo-2 ethyl>phenobarbital is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124558-99-2 Structure
  • Basic information

    1. Product Name: N1,N3-di<(adamantyl-1)-2 oxo-2 ethyl>phenobarbital
    2. Synonyms: N1,N3-di<(adamantyl-1)-2 oxo-2 ethyl>phenobarbital
    3. CAS NO:124558-99-2
    4. Molecular Formula:
    5. Molecular Weight: 584.756
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124558-99-2.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: N1,N3-di<(adamantyl-1)-2 oxo-2 ethyl>phenobarbital(CAS DataBase Reference)
    10. NIST Chemistry Reference: N1,N3-di<(adamantyl-1)-2 oxo-2 ethyl>phenobarbital(124558-99-2)
    11. EPA Substance Registry System: N1,N3-di<(adamantyl-1)-2 oxo-2 ethyl>phenobarbital(124558-99-2)
  • 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: 124558-99-2(Hazardous Substances Data)

124558-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124558-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,5 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124558-99:
(8*1)+(7*2)+(6*4)+(5*5)+(4*5)+(3*8)+(2*9)+(1*9)=142
142 % 10 = 2
So 124558-99-2 is a valid CAS Registry Number.

124558-99-2Downstream Products

124558-99-2Relevant articles and documents

Synthese de pyrimidines et purines adamantylees par alkylation regioselective directe, an catalyse par transfert de phase

Hedayatullah, Mir,Roger, Annie

, p. 1093 - 1096 (2007/10/02)

The use of 1-adamantyl bromomethyl ketone, under phase transfer catalysis conditions, permits the regioselective N1-alkylation of uracil and thymine, the N9-alkylation of adenine and 8-azaadenine and the N7-alkylation of t

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