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1262018-03-0

1-(benzyloxy)-3-methylheptan-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1262018-03-0 Structure

  • Basic information

    1. Product Name: 1-(benzyloxy)-3-methylheptan-4-one
    2. Synonyms: 1-(benzyloxy)-3-methylheptan-4-one
    3. CAS NO:1262018-03-0
    4. Molecular Formula:
    5. Molecular Weight: 234.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1262018-03-0.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: 1-(benzyloxy)-3-methylheptan-4-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(benzyloxy)-3-methylheptan-4-one(1262018-03-0)
    11. EPA Substance Registry System: 1-(benzyloxy)-3-methylheptan-4-one(1262018-03-0)

  • 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: 1262018-03-0(Hazardous Substances Data)

1262018-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1262018-03-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,0,1 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1262018-03:
(9*1)+(8*2)+(7*6)+(6*2)+(5*0)+(4*1)+(3*8)+(2*0)+(1*3)=110
110 % 10 = 0
So 1262018-03-0 is a valid CAS Registry Number.

1262018-03-0Upstream product

1262018-03-0Downstream Products

1262018-03-0Relevant articles and documents

Synthesis of α-methyl ketones by a selective, iridium-catalyzed cyclopropanol ring-opening reaction

Ziegler, Daniel T.,Steffens, Andrew M.,Funk, Timothy W.

, p. 6726 - 6729 (2010)

A mild method for synthesizing α-methyl ketones from substituted cyclopropanols is reported. This process, catalyzed by [CpIrCl2] 2, cleaves cyclopropanol rings regioselectively and more efficiently than the other conditions examined. While tertiary cyclopropanols afford α-methyl ketones, secondary cyclopropanols and cyclopropyl silyl ethers are less reactive and yield other isomerization products.

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