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(3beta,5beta)-3-[(6-deoxy-4-O-beta-D-glucopyranosyl-alpha-L-mannopyranosyl)oxy]-5,14-dihydroxy-19-oxocard-20(22)-enolide is a complex cardenolide glycoside with a steroid structure and multiple hydroxyl groups and sugar moieties attached. It is derived from natural sources and has been studied for its potential pharmacological effects such as anticancer, anti-inflammatory, and cardiovascular activities. Its specific chemical structure and properties make it a subject of interest in drug discovery and development.

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  • Card-20(22)-enolide,3-[(6-deoxy-4-O-b-D-glucopyranosyl-a-L-mannopyranosyl)oxy]-5,14-dihydroxy-19-oxo-,(3b,5b)- (9CI)

    Cas No: 13473-51-3

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  • (3beta,5beta)-3-[(6-deoxy-4-O-beta-D-glucopyranosyl-alpha-L-mannopyranosyl)oxy]-5,14-dihydroxy-19-oxocard-20(22)-enolide

    Cas No: 13473-51-3

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  • Card-20(22)-enolide,3-[(6-deoxy-4-O-b-D-glucopyranosyl-a-L-mannopyranosyl)oxy]-5,14-dihydroxy-19-oxo-,(3b,5b)- (9CI)

    Cas No: 13473-51-3

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  • 13473-51-3 Structure
  • Basic information

    1. Product Name: (3beta,5beta)-3-[(6-deoxy-4-O-beta-D-glucopyranosyl-alpha-L-mannopyranosyl)oxy]-5,14-dihydroxy-19-oxocard-20(22)-enolide
    2. Synonyms: (3beta,5beta)-3-[(6-deoxy-4-O-beta-D-glucopyranosyl-alpha-L-mannopyranosyl)oxy]-5,14-dihydroxy-19-oxocard-20(22)-enolide;convalloside;3β-[(4-O-β-D-Glucopyranosyl-6-deoxy-α-L-mannopyranosyl)oxy]-5,14-dihydroxy-19-oxo-5β-card-20(22)-enolide
    3. CAS NO:13473-51-3
    4. Molecular Formula: C35H52O15
    5. Molecular Weight: 712.77838
    6. EINECS: 236-749-7
    7. Product Categories: N/A
    8. Mol File: 13473-51-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 927.8°Cat760mmHg
    3. Flash Point: 288.6°C
    4. Appearance: /
    5. Density: 1.5g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (3beta,5beta)-3-[(6-deoxy-4-O-beta-D-glucopyranosyl-alpha-L-mannopyranosyl)oxy]-5,14-dihydroxy-19-oxocard-20(22)-enolide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3beta,5beta)-3-[(6-deoxy-4-O-beta-D-glucopyranosyl-alpha-L-mannopyranosyl)oxy]-5,14-dihydroxy-19-oxocard-20(22)-enolide(13473-51-3)
    11. EPA Substance Registry System: (3beta,5beta)-3-[(6-deoxy-4-O-beta-D-glucopyranosyl-alpha-L-mannopyranosyl)oxy]-5,14-dihydroxy-19-oxocard-20(22)-enolide(13473-51-3)
  • 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: 13473-51-3(Hazardous Substances Data)

13473-51-3 Usage

Uses

Used in Pharmaceutical Industry:
(3beta,5beta)-3-[(6-deoxy-4-O-beta-D-glucopyranosyl-alpha-L-mannopyranosyl)oxy]-5,14-dihydroxy-19-oxocard-20(22)-enolide is used as a pharmaceutical agent for its potential anticancer, anti-inflammatory, and cardiovascular activities. Its unique chemical structure and properties make it a promising candidate for drug discovery and development.
Used in Drug Delivery Systems:
(3beta,5beta)-3-[(6-deoxy-4-O-beta-D-glucopyranosyl-alpha-L-mannopyranosyl)oxy]-5,14-dihydroxy-19-oxocard-20(22)-enolide can be used in drug delivery systems to improve the delivery, bioavailability, and therapeutic outcomes of the compound. Various organic and metallic nanoparticles can be employed as carriers for the delivery of this complex cardenolide glycoside, enhancing its efficacy in treating various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 13473-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,7 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13473-51:
(7*1)+(6*3)+(5*4)+(4*7)+(3*3)+(2*5)+(1*1)=93
93 % 10 = 3
So 13473-51-3 is a valid CAS Registry Number.

13473-51-3Downstream Products

13473-51-3Relevant articles and documents

SYNTHESIS OF CONVALLOSIDE

Makarevich, I. F.,Terno, I. S.

, p. 323 - 325 (2007/10/02)

The known natural diglycoside convalloside - strophanthidin 3β-O- - has been synthesized.The synthesis was carried out by the Koenigs-Knorr method via the preparation as intermediates of convallatoxin and its 2,3-isopropylidene derivative.Selectivity of glycosylation was achieved by the preliminary protection of the two OH groups in the cardenolide L-rhamnoside (convallatoxin).

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