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114-42-1

Flavaspidic acid is a natural organic compound predominantly found in the Asclepiadaceae family of plants, characterized by its notable antibacterial properties. It is recognized for its effectiveness against a range of bacterial strains, including those that are drug-resistant, which positions it as a potential candidate for the development of novel antibiotics. Beyond its antibacterial capabilities, flavaspidic acid also displays anti-inflammatory and anti-tumor properties, suggesting its potential as a multifaceted therapeutic agent for a variety of medical conditions.

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  • 2,5-Cyclohexadien-1-one,3,5-dihydroxy-4,4-dimethyl-2-(1-oxobutyl)-6-[[2,4,6-trihydroxy-3-methyl-5-(1-oxobutyl)phenyl]methyl]-

    Cas No: 114-42-1

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  • 2,5-Cyclohexadien-1-one,3,5-dihydroxy-4,4-dimethyl-2-(1-oxobutyl)-6-[[2,4,6-trihydroxy-3-methyl-5-(1-oxobutyl)phenyl]methyl]-

    Cas No: 114-42-1

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  • 2,5-Cyclohexadien-1-one,3,5-dihydroxy-4,4-dimethyl-2-(1-oxobutyl)-6-[[2,4,6-trihydroxy-3-methyl-5-(1-oxobutyl)phenyl]methyl]-

    Cas No: 114-42-1

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  • 2-butanoyl-4-[(3-butanoyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-3,5-dihydroxy-6,6-dimethylcyclohexa-2,4-dien-1-one

    Cas No: 114-42-1

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  • 114-42-1 Structure

  • Basic information

    1. Product Name: flavaspidic acid
    2. Synonyms: flavaspidic acid;3,5-Dihydroxy-4,4-dimethyl-2-(1-oxobutyl)-6-[[2,4,6-trihydroxy-3-methyl-5-(1-oxobutyl)phenyl]methyl]-2,5-cyclohexadien-1-one;3,5-Dihydroxy-4,4-dimethyl-2-(1-oxobutyl)-6-[[2,4,6-trihydroxy-3-methyl-5-(1-oxobutyl)phenyl]methyl]-2,5-cyclohexadiene-1-one;Flavaspidic acid BB;Polystichocitrin;Toxifren
    3. CAS NO:114-42-1
    4. Molecular Formula: C24H30O8
    5. Molecular Weight: 446.493
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114-42-1.mol

  • Chemical Properties

    1. Melting Point: 92°C
    2. Boiling Point: 475.85°C (rough estimate)
    3. Flash Point: 404.3°C
    4. Appearance: /
    5. Density: 1.1947 (rough estimate)
    6. Vapor Pressure: 1.56E-21mmHg at 25°C
    7. Refractive Index: 1.4480 (estimate)
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: flavaspidic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: flavaspidic acid(114-42-1)
    12. EPA Substance Registry System: flavaspidic acid(114-42-1)

  • 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: 114-42-1(Hazardous Substances Data)

114-42-1 Usage

Uses

Used in Pharmaceutical Industry:
Flavaspidic acid is used as an antibacterial agent for its broad-spectrum efficacy against various bacterial strains, including drug-resistant ones, making it a valuable resource in the fight against antibiotic-resistant infections.
Used in Anti-inflammatory Applications:
Flavaspidic acid is utilized as an anti-inflammatory agent due to its ability to reduce inflammation, which can be beneficial in treating conditions characterized by excessive inflammation.
Used in Oncology:
Flavaspidic acid is employed as an anti-tumor agent for its potential to combat tumor growth, offering a natural alternative in cancer treatment strategies.
Further research is essential to fully elucidate the mechanisms of action of flavaspidic acid and to explore its potential applications in medicine and healthcare, ensuring its safe and effective use in various therapeutic areas.

Check Digit Verification of cas no

The CAS Registry Mumber 114-42-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 114-42:
(5*1)+(4*1)+(3*4)+(2*4)+(1*2)=31
31 % 10 = 1
So 114-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C24H30O8/c1-6-8-14(25)16-19(28)11(3)18(27)12(20(16)29)10-13-21(30)17(15(26)9-7-2)23(32)24(4,5)22(13)31/h27-31H,6-10H2,1-5H3

114-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butanoyl-4-[(3-butanoyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-3,5-dihydroxy-6,6-dimethylcyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names Flavaspidsaeure

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:114-42-1 SDS

114-42-1Downstream Products

114-42-1Related news

Inhibition of porcine reproductive and respiratory syndrome virus replication by flavaspidic acid (cas 114-42-1) AB08/21/2019

Porcine reproductive and respiratory syndrome virus (PRRSV) represents a significant challenge to the swine industry worldwide. Current control strategies against PRRSV are still inadequate and there is an urgent need for new antiviral therapies. Flavaspidic acid AB (FA-AB) is a compound derived...detailed

114-42-1Relevant articles and documents

A natural product yellow filicic acid BB of full-synthesis method

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, (2019/01/08)

The invention relates to a natural product yellow filicic acid BB of full-synthesis method, which belongs to the technical field of organic chemistry. The invention from the economic and easy to synthesize the phloroglucinol proceed double-acylated phloroglucinol, then after iodine methane-to-carbon double methylation, removing monomolecular acyl got the midbody 3; to phloroglucinol as raw materials, acetate acylation to obtain the aldehyde phloroglucinol, reduction of the aldehyde is methyl, then acylated to obtain intermediate 6; the two fragments obtained through the Eschenmoser's salt combined yellow filicic acid BB. In the method 42% overall yield of yellow filicic acid improves the BB fully synthetic yield, raw material economy are easy, simple operation, high yield, and suitable for production, may be its biological activity study provide a large number of raw materials.

Dryopteris fragrans phloroglucinol compound flavaspidic acid BB and antibacterial application thereof

-

, (2018/05/24)

The invention relates to the technical field of medicine and discloses an antibacterial application of a Dryopteris fragrans phloroglucinol compound flavaspidic acid BB. The invention provides the flavaspidic acid BB obtained by the chemical synthesis method. The flavaspidic acid BB has good antibacterial effects, effectively fills in the application deficiency of the antibacterial natural compound and provides an effective antibacterial solution for drug-resistant bacteria. The experimental results show that the compound has a strong antibacterial effect and good curative effects especially on drug-resistant bacteria.

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