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CAS

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1293375-06-0

8β,13β-dihydroxy-13α-4'-chloro-2'-methylphenylpodocarpane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1293375-06-0 Structure

  • Basic information

    1. Product Name: 8β,13β-dihydroxy-13α-4'-chloro-2'-methylphenylpodocarpane
    2. Synonyms: 8β,13β-dihydroxy-13α-4'-chloro-2'-methylphenylpodocarpane
    3. CAS NO:1293375-06-0
    4. Molecular Formula:
    5. Molecular Weight: 390.994
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1293375-06-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 8β,13β-dihydroxy-13α-4'-chloro-2'-methylphenylpodocarpane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8β,13β-dihydroxy-13α-4'-chloro-2'-methylphenylpodocarpane(1293375-06-0)
    11. EPA Substance Registry System: 8β,13β-dihydroxy-13α-4'-chloro-2'-methylphenylpodocarpane(1293375-06-0)

  • 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: 1293375-06-0(Hazardous Substances Data)

1293375-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1293375-06-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,3,3,7 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1293375-06:
(9*1)+(8*2)+(7*9)+(6*3)+(5*3)+(4*7)+(3*5)+(2*0)+(1*6)=170
170 % 10 = 0
So 1293375-06-0 is a valid CAS Registry Number.

1293375-06-0Downstream Products

1293375-06-0Relevant articles and documents

Synthesis and anti-plasmodial activity of 8β, 13β- Dihydroxypodocarpane derivatives

Young, Ryan M.,Popplewell, Wendy L.,Caira, Mino R.,Van Zyl, Robyn L.,Davies-Coleman, Michael T.

, p. 18 - 23 (2011/05/04)

8β,13β-Dihydroxypodocarpane and eight C-13 substituted derivatives were prepared from the precursor 8bhydroxy-13-podocarpanone synthesised from the naturally occurring diterpene (+)-manool. The synthetic compounds exhibited a range of anti-plasmodial activities (IC50 1-29 μM) and only induced minimal haemolysis of erythrocytes at concentrations 50 and 100 μM. No changes in the morphology of erythrocytes were detected at sub-haemolytic concentrations.

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