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18196-13-9

Naringenin-4',7-diacetate is a chemical compound derived from naringenin, a flavonoid present in citrus fruits like grapefruits and oranges. It is formed by the acetylation of naringenin, which involves the addition of acetyl groups to the 4' and 7 positions of the molecule. This modification enhances the stability, bioavailability, and potential biological activities of naringenin. Naringenin-4',7-diacetate has been studied for its antioxidant, anti-inflammatory, and anti-cancer properties, making it a promising candidate for the treatment and prevention of various health conditions. Its therapeutic potential is currently under investigation in the fields of pharmacology and medicine.

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  • 18196-13-9 Structure

  • Basic information

    1. Product Name: Naringenin-4',7-diacetate
    2. Synonyms: Naringenin-4',7-diacetate;(S)-4',5,7-Trihydroxyflavanone 4',7-diacetate;4-(7-Acetoxy-5-hydroxy-4-oxochroman-2-yl)phenyl acetate;Naringenin 7,4'-diacetate
    3. CAS NO:18196-13-9
    4. Molecular Formula: C19H16O7
    5. Molecular Weight: 356
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 18196-13-9.mol

  • Chemical Properties

    1. Melting Point: 140-142 °C
    2. Boiling Point: 578.9±50.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.361±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 7.00±0.40(Predicted)
    10. CAS DataBase Reference: Naringenin-4',7-diacetate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Naringenin-4',7-diacetate(18196-13-9)
    12. EPA Substance Registry System: Naringenin-4',7-diacetate(18196-13-9)

  • 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: 18196-13-9(Hazardous Substances Data)

18196-13-9 Usage

Uses

Used in Pharmaceutical Industry:
Naringenin-4',7-diacetate is used as a pharmaceutical agent for its antioxidant, anti-inflammatory, and anti-cancer properties. It has the potential to treat and prevent various health conditions by modulating biological pathways and reducing oxidative stress.
Used in Nutraceutical Industry:
Naringenin-4',7-diacetate is used as a nutraceutical ingredient to enhance the health benefits of dietary supplements and functional foods. Its antioxidant and anti-inflammatory properties can contribute to overall health and well-being.
Used in Cosmetic Industry:
Naringenin-4',7-diacetate is used as an active ingredient in cosmetic products for its potential skin health benefits. Its antioxidant and anti-inflammatory properties may help protect the skin from environmental damage and promote a healthy complexion.
Used in Research and Development:
Naringenin-4',7-diacetate is used as a subject of ongoing research in the fields of pharmacology and medicine. Its potential therapeutic benefits are being investigated for various health conditions, and new applications may be discovered as research progresses.

Check Digit Verification of cas no

The CAS Registry Mumber 18196-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,9 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18196-13:
(7*1)+(6*8)+(5*1)+(4*9)+(3*6)+(2*1)+(1*3)=119
119 % 10 = 9
So 18196-13-9 is a valid CAS Registry Number.

18196-13-9SDS

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 [4-(7-acetyloxy-5-hydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenyl] acetate

1.2 Other means of identification

Product number -
Other names Naringenin-4',7-diacetate

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:18196-13-9 SDS

18196-13-9Downstream Products

18196-13-9Relevant articles and documents

A practical access to highly enantiomerically pure flavanones by catalytic asymmetric transfer hydrogenation

Lemke, Marie-Kristin,Schwab, Pia,Fischer, Petra,Tischer, Sandra,Witt, Morris,Noehringer, Laurence,Rogachev, Victor,Jaeger, Anne,Kataeva, Olga,Froehlich, Roland,Metz, Peter

supporting information, p. 11651 - 11655 (2013/11/06)

A surprisingly selective, non-enzymatic kinetic resolution of readily available, racemic β-chiral ketones enabled the title process, which was applied to a rapid synthesis of several bioactive flavanones in virtually enantiopure form (see scheme; MOM=methoxymethyl, Ts=p-toluenesulfonyl). Copyright

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