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59979-57-6

Tagitinin F, a sesquiterpene lactone, is a natural chemical compound extracted from the leaves of the Tithonia diversifolia plant, also known as the Mexican sunflower. It is recognized for its anti-inflammatory, antimicrobial, and anticancer properties, with ongoing research exploring its potential in various medical applications, particularly in cancer therapy.

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  • Propanoic acid,2-methyl-,(3aR,4R,6R,9R,10Z,11aR)-2,3,3a,4,5,6,9,11a-octahydro-9-hydroxy-6,10-dimethyl-3-methylene-2-oxo-6,9-epoxycyclodeca[b]furan-4-ylester

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  • Propanoic acid,2-methyl-,(3aR,4R,6R,9R,10Z,11aR)-2,3,3a,4,5,6,9,11a-octahydro-9-hydroxy-6,10-dimethyl-3-methylene-2-oxo-6,9-epoxycyclodeca[b]furan-4-ylester

    Cas No: 59979-57-6

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  • 59979-57-6 Structure

  • Basic information

    1. Product Name: Tagitinin F
    2. Synonyms: Tagitinin F
    3. CAS NO:59979-57-6
    4. Molecular Formula: C19H24O6
    5. Molecular Weight: 348.3903
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 59979-57-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 512.9°Cat760mmHg
    3. Flash Point: 181.1°C
    4. Appearance: /
    5. Density: 1.24g/cm3
    6. Vapor Pressure: 1.15E-12mmHg at 25°C
    7. Refractive Index: 1.557
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Tagitinin F(CAS DataBase Reference)
    11. NIST Chemistry Reference: Tagitinin F(59979-57-6)
    12. EPA Substance Registry System: Tagitinin F(59979-57-6)

  • 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: 59979-57-6(Hazardous Substances Data)

59979-57-6 Usage

Uses

Used in Cancer Therapy:
Tagitinin F is used as a cytotoxic and antiproliferative agent for its potential in cancer treatment. It has demonstrated promising effects on cancer cells, making it a candidate for further exploration in oncological research.
Used in Anti-Inflammatory Applications:
In the field of anti-inflammatory treatments, Tagitinin F is used as an agent to reduce inflammation and alleviate pain due to its observed anti-inflammatory and analgesic properties.
Used in Antimicrobial Applications:
Tagitinin F is utilized as an antimicrobial agent, contributing to the fight against infections by inhibiting the growth of various microorganisms.
Used in Drug Development:
As research progresses, Tagitinin F may be incorporated into drug development for targeted therapies, particularly in the areas of cancer, inflammation, and infectious diseases, due to its multifaceted biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 59979-57-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,7 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59979-57:
(7*5)+(6*9)+(5*9)+(4*7)+(3*9)+(2*5)+(1*7)=206
206 % 10 = 6
So 59979-57-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H24O6/c1-10(2)16(20)24-14-9-18(5)6-7-19(22,25-18)11(3)8-13-15(14)12(4)17(21)23-13/h6-8,10,13-15,22H,4,9H2,1-3,5H3/b11-8-/t13-,14-,15+,18+,19-/m1/s1

59979-57-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Tagitinin F

1.2 Other means of identification

Product number -
Other names tagitinin-F

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

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More Details:59979-57-6 SDS

59979-57-6Downstream Products

59979-57-6Relevant articles and documents

PHOTOCYCLIZATION OF A HELIANGOLIDE - A CYCLODECADIENONE

Chowdhury, P. K.,Sharma, R. P.,Baruah, J. N.

, p. 5429 - 5432 (1983)

Irradiation of the dienone 1 furnishes essentially a single tricyclic product 2 containing cyclobutane ring.The corresponding epoxide 5 furnishes tagitinin F 6 - an antileukemic compound.

Absolute Stereochemistry of Tagitinin-F

Chowdhury, P. K.,Sharma, R. P.,Barua, J. N.

, p. 402 (2007/10/02)

Absolute stereochemistry of tagitinin-F has been established by photochemical transformation of tagitinin-C to tagitinin-F.

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