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  • 24959-84-0 Structure
  • Basic information

    1. Product Name: Canin
    2. Synonyms: Canin;(3aS,6aR)-3aβ,5,6,7aα,7bα,8a,8bβ,8cα-Octahydro-6β-hydroxy-6,8aα-dimethyl-3-methylene-4H-bisoxireno[1,8a:2,3]azuleno[4,5-b]furan-2(3H)-one;Chrysartemin A
    3. CAS NO:24959-84-0
    4. Molecular Formula: C15H18O5
    5. Molecular Weight: 278.30042
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24959-84-0.mol
  • Chemical Properties

    1. Melting Point: 245-246 °C
    2. Boiling Point: 487.2°Cat760mmHg
    3. Flash Point: 187.8°C
    4. Appearance: /
    5. Density: 1.43g/cm3
    6. Vapor Pressure: 1.54E-11mmHg at 25°C
    7. Refractive Index: 1.611
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 14.77±0.40(Predicted)
    11. CAS DataBase Reference: Canin(CAS DataBase Reference)
    12. NIST Chemistry Reference: Canin(24959-84-0)
    13. EPA Substance Registry System: Canin(24959-84-0)
  • 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: 24959-84-0(Hazardous Substances Data)

24959-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24959-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,5 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24959-84:
(7*2)+(6*4)+(5*9)+(4*5)+(3*9)+(2*8)+(1*4)=150
150 % 10 = 0
So 24959-84-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H18O5/c1-6-7-4-5-13(2,17)15-9(8(7)18-12(6)16)14(3)10(19-14)11(15)20-15/h7-11,17H,1,4-5H2,2-3H3/t7-,8-,9-,10+,11-,13+,14-,15+/m0/s1

24959-84-0Upstream product

24959-84-0Downstream Products

24959-84-0Relevant articles and documents

Sesquiterpene lactones from feverfew, Tanacetum parthenium: Isolation, structural revision, activity against human blood platelet function and implications for migraine therapy

Hewlett, Martin J.,Begley, Michael J.,Groenewegen, W. Antoinette,Heptinstall, Stan,Knight, David W.,May, Jane,Salan, Umit,Toplis, Dane

, p. 1979 - 1986 (1996)

The structures of two series of sesquiterpene lactones (the 'α'-series 11, 12 and 16 and the 'β'-series 15, 17 and 18) present in the herb feverfew have been revised in the light of both X-ray analysis and chemical correlations. A biosynthetic pathway is proposed, involving a Diels-Alder type addition of oxygen followed by two contrasting rearrangements, starting from a common intermediate, the cyclopentadiene 19, which has not been identified in feverfew extracts but which is related to a recently isolated structure. The activity of some of these metabolites as well as of the major sesquiterpene lactone present in feverfew, parthenolide 2, and some simpler synthetic models as inhibitors of human blood platelet function has been determined. The possible relevance of this effect to migraine prophylaxis by feverfew is briefly discussed.

REVISED STRUCTURES FOR GUAIANOLIDE α-METHYLENEBUTYROLACTONES FROM FEVERFEW

Begley, Michael J.,Hewlett, Martin J.,Knight, David W.

, p. 940 - 943 (1989)

The structures of two series of guaianolides present in feverfew, Tanacetum parthenium, are established as tanaparthin-α-peroxide, canin and seco-tanapartholide-A and the corresponding 'β'-series using a combination of spectroscopic and X-ray crystallographic analyses and chemical transformations.Key Word Index - Tanacetum parthenium; Compositae; feverfew; sesquiterpene lactones; parthenolide; guaianolides; migraine.

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