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130836-56-5

5-benzyl-1-methyl-4-O-methyl tetramate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130836-56-5 Structure

  • Basic information

    1. Product Name: 5-benzyl-1-methyl-4-O-methyl tetramate
    2. Synonyms: 5-benzyl-1-methyl-4-O-methyl tetramate
    3. CAS NO:130836-56-5
    4. Molecular Formula:
    5. Molecular Weight: 217.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130836-56-5.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: 5-benzyl-1-methyl-4-O-methyl tetramate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-benzyl-1-methyl-4-O-methyl tetramate(130836-56-5)
    11. EPA Substance Registry System: 5-benzyl-1-methyl-4-O-methyl tetramate(130836-56-5)

  • 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: 130836-56-5(Hazardous Substances Data)

130836-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130836-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,8,3 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130836-56:
(8*1)+(7*3)+(6*0)+(5*8)+(4*3)+(3*6)+(2*5)+(1*6)=115
115 % 10 = 5
So 130836-56-5 is a valid CAS Registry Number.

130836-56-5Relevant articles and documents

New Protocols for the Synthesis of Substituted 4-O-Methyl Tetramates

Jones, Raymond C. F.,Patience, Jacqueline M.

, p. 2350 - 2351 (2007/10/02)

The deprotonation behaviour of 4-methoxypyrrol-2(5H)-ones (4-O-methyl tetramates) is defined and exploited to provide methods for the synthesis of methyl tetramates variously substituted at N-1, C-5, and C-3.

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