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5-benzyloxy-1-diazo-4-methoxypentan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 444992-09-0 Structure
  • Basic information

    1. Product Name: 5-benzyloxy-1-diazo-4-methoxypentan-2-one
    2. Synonyms:
    3. CAS NO:444992-09-0
    4. Molecular Formula:
    5. Molecular Weight: 248.282
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 444992-09-0.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: 5-benzyloxy-1-diazo-4-methoxypentan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-benzyloxy-1-diazo-4-methoxypentan-2-one(444992-09-0)
    11. EPA Substance Registry System: 5-benzyloxy-1-diazo-4-methoxypentan-2-one(444992-09-0)
  • 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: 444992-09-0(Hazardous Substances Data)

444992-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 444992-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,9,9 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 444992-09:
(8*4)+(7*4)+(6*4)+(5*9)+(4*9)+(3*2)+(2*0)+(1*9)=180
180 % 10 = 0
So 444992-09-0 is a valid CAS Registry Number.

444992-09-0Downstream Products

444992-09-0Relevant articles and documents

Cyclic oxonium ylides: Building blocks for iterative synthesis of polycyclic ethers

Marms?ter, Fredrik P,Vanecko, John A,West

, p. 2027 - 2040 (2007/10/03)

A series of diazoketones bearing remote benzyl or allyl ethers was subjected to a variety of conditions for catalytic diazodecomposition and cyclic oxonium ylide formation as a possible method for polycyclic ether synthesis. Allyl ethers 19, 25 and 29 und

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