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6-acetoxy-2-methoxy-3-methyl-cyclohex-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 148646-82-6 Structure
  • Basic information

    1. Product Name: 6-acetoxy-2-methoxy-3-methyl-cyclohex-2-en-1-one
    2. Synonyms:
    3. CAS NO:148646-82-6
    4. Molecular Formula:
    5. Molecular Weight: 198.219
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148646-82-6.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: 6-acetoxy-2-methoxy-3-methyl-cyclohex-2-en-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-acetoxy-2-methoxy-3-methyl-cyclohex-2-en-1-one(148646-82-6)
    11. EPA Substance Registry System: 6-acetoxy-2-methoxy-3-methyl-cyclohex-2-en-1-one(148646-82-6)
  • 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: 148646-82-6(Hazardous Substances Data)

148646-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148646-82-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,6,4 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 148646-82:
(8*1)+(7*4)+(6*8)+(5*6)+(4*4)+(3*6)+(2*8)+(1*2)=166
166 % 10 = 6
So 148646-82-6 is a valid CAS Registry Number.

148646-82-6Relevant articles and documents

The α'-oxidation of α-alkoxy enones using manganese(III) acetate in combination with carboxylic acids

Demir,Saatcioglu

, p. 571 - 575 (1993)

The α'-oxidation of cyclic derivatives of α-alkoxy-α,β-unsaturated ketones using manganese(III)acetate in the presence of various carboxylic acids provided a convenient synthesis of 5-acyloxy-2-alkoxy-2-cyclopentenones and 6-acyloxy-2-alkoxy-2-cyclohexeno

A new and efficient chemoenzymatic route to both enantiomers of α′-acetoxy and α′-hydroxy-α-methoxy cyclic enones

Demir, Ayhan S.,Caliskan, Zerrin,Aydin, A. Ebru,Bicer, Isil

, p. 786 - 791 (2007/10/03)

A chemoenzymatic synthesis of both enantiomers of the pharmacologically interesting α′-acetoxy and α′-hydroxy-α-methoxy cyclic enones starting from α-hydroxy cyclic enones is described. Protection of 1,2-diketones, manganese(III) acetate-mediated acetoxyl

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