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132017-99-3

Methyl 3-(2-Hydroxy-5-methoxyphenyl)-3-oxopropanoate is a yellow solid that serves as a valuable synthetic intermediate in the preparation of flavonoids, a group of naturally occurring compounds with diverse biological activities.
Used in Pharmaceutical Industry:
Methyl 3-(2-Hydroxy-5-methoxyphenyl)-3-oxopropanoate is used as a synthetic intermediate for the production of flavonoids, which are known for their potential health benefits and therapeutic applications. These flavonoids can be utilized in the development of drugs and supplements targeting various health conditions.
Used in Cosmetic Industry:
In the cosmetic industry, Methyl 3-(2-Hydroxy-5-methoxyphenyl)-3-oxopropanoate is used as a synthetic intermediate for the creation of flavonoid-based compounds that possess antioxidant, anti-inflammatory, and skin protective properties, making them suitable for inclusion in skincare products.
Used in Food and Beverage Industry:
Methyl 3-(2-Hydroxy-5-methoxyphenyl)-3-oxopropanoate is used as a synthetic intermediate in the development of flavonoid-enriched food and beverage products, capitalizing on the health-promoting properties of flavonoids to enhance the nutritional value and appeal of these products.

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  • 132017-99-3 Structure

  • Basic information

    1. Product Name: Methyl 3-(2-Hydroxy-5-methoxyphenyl)-3-oxopropanoate
    2. Synonyms: 2-Hydroxy-5-Methoxy-β-oxo-benzenepropanoic Acid Methyl Ester
    3. CAS NO:132017-99-3
    4. Molecular Formula: C11H12O5
    5. Molecular Weight: 224.21
    6. EINECS: N/A
    7. Product Categories: Various Intermediates;Aromatics;Intermediates
    8. Mol File: 132017-99-3.mol

  • Chemical Properties

    1. Melting Point: 48-49°C
    2. Boiling Point: 329.2±27.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.246±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: -20°C Freezer
    8. Solubility: N/A
    9. PKA: 8.19±0.43(Predicted)
    10. CAS DataBase Reference: Methyl 3-(2-Hydroxy-5-methoxyphenyl)-3-oxopropanoate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Methyl 3-(2-Hydroxy-5-methoxyphenyl)-3-oxopropanoate(132017-99-3)
    12. EPA Substance Registry System: Methyl 3-(2-Hydroxy-5-methoxyphenyl)-3-oxopropanoate(132017-99-3)

  • 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: 132017-99-3(Hazardous Substances Data)

132017-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132017-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,1 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132017-99:
(8*1)+(7*3)+(6*2)+(5*0)+(4*1)+(3*7)+(2*9)+(1*9)=93
93 % 10 = 3
So 132017-99-3 is a valid CAS Registry Number.

132017-99-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-(2-Hydroxy-5-methoxyphenyl)-3-oxopropanoate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:132017-99-3 SDS

132017-99-3Relevant articles and documents

Synthesis and Protein-Tyrosine Kinase Inhibitory Activities of Flavanoid Analogues

Cushman, Mark,Nagarathnam, Dhanapalan,Burg, Debra L.,Geahlen, Robert L.

, p. 798 - 806 (2007/10/02)

Treatment of o-hydroxyacetophenones 2a-e with excess lithium bis(trimethylsilyl)amide followed by dialkyl carbonates gave 3-(2-hydroxyaryl)-3-oxopropanoates 3a-e.The latter substances were transformed through the reaction of their magnesium chelates with

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