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6953-31-7

2-acetyl-3,5,6-trimethoxyphenyl acetate is a complex organic compound with the molecular formula C13H16O6. It is characterized by a phenyl ring with three methoxy groups attached to the 3rd, 5th, and 6th carbon atoms, and an acetyl group at the 2nd carbon. Additionally, the molecule features an acetate group esterified to the phenyl ring. 2-acetyl-3,5,6-trimethoxyphenyl acetate is known for its potential applications in the synthesis of various pharmaceuticals and natural products due to its unique structure and reactivity. It is typically synthesized through multi-step organic reactions and is used as an intermediate in the preparation of more complex molecules. The compound's properties, such as its solubility and stability, are influenced by the presence of the electron-donating methoxy groups and the electron-withdrawing acetyl group, making it a versatile building block in organic chemistry.

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  • 6953-31-7 Structure

  • Basic information

    1. Product Name: 2-acetyl-3,5,6-trimethoxyphenyl acetate
    2. Synonyms:
    3. CAS NO:6953-31-7
    4. Molecular Formula: C13H16O6
    5. Molecular Weight: 268.2625
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6953-31-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 387°C at 760 mmHg
    3. Flash Point: 171.1°C
    4. Appearance: N/A
    5. Density: 1.163g/cm3
    6. Vapor Pressure: 3.4E-06mmHg at 25°C
    7. Refractive Index: 1.498
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-acetyl-3,5,6-trimethoxyphenyl acetate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-acetyl-3,5,6-trimethoxyphenyl acetate(6953-31-7)
    12. EPA Substance Registry System: 2-acetyl-3,5,6-trimethoxyphenyl acetate(6953-31-7)

  • 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: 6953-31-7(Hazardous Substances Data)

6953-31-7 Usage

Class

Phenolic compound

Derivative of

Acetanisole

Properties

Antioxidant: Potential antioxidant properties
Antifungal: Known for antifungal properties

Applications

Pharmaceutical Industry: Studied for potential pharmaceutical applications
Food Industry: Investigated for potential uses in food industry

Synthesis

Used in synthesis of various pharmaceutical drugs
Utilized in synthesis of natural products

Research

Investigated for development of new drugs
Potential role in treating various diseases

Check Digit Verification of cas no

The CAS Registry Mumber 6953-31-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6953-31:
(6*6)+(5*9)+(4*5)+(3*3)+(2*3)+(1*1)=117
117 % 10 = 7
So 6953-31-7 is a valid CAS Registry Number.

6953-31-7Relevant articles and documents

Improved, rapid and efficient synthesis of polymethoxyflavones under microwave irradiation and their inhibitory effects on melanogenesis

Tsukayama, Masao,Kawamura, Yasuhiko,Ishizuka, Takaaki,Hayashi, Shinji,Torii, Fumihito

, p. 2775 - 2784 (2007/10/03)

The microwave-assisted methylation of 2,5-dihydroxy-1,3-dimethoxybenzene with (CH3O)2SO2 for 5 min gave easily 1,2,3,5-tetramethoxybenzene, which was converted into pentamethoxybenzene. The microwave-assisted Friedel-Crafts acylation of pentamethoxybenzene in the presence of In(CF3SO3)3 gave pentamethoxyacetophenone for 15 min under solvent-free conditions in high yield. The microwave-assisted cyclization reaction of the diketones, which were synthesized from the acetophenone via three steps under microwave irradiation, gave the desired polymethoxyflavones for 1.5-3 min in high yields. The polymethoxyflavones showed inhibitory effects on melanogenesis in a human melanoma.

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