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1315567-67-9

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  • 1315567-67-9 Structure

  • Basic information

    1. Product Name: C36H56O7Si2
    2. Synonyms: C36H56O7Si2
    3. CAS NO:1315567-67-9
    4. Molecular Formula:
    5. Molecular Weight: 657.007
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1315567-67-9.mol
    9. Article Data: 1

  • 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: C36H56O7Si2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C36H56O7Si2(1315567-67-9)
    11. EPA Substance Registry System: C36H56O7Si2(1315567-67-9)

  • 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: 1315567-67-9(Hazardous Substances Data)

1315567-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1315567-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,5,6 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1315567-67:
(9*1)+(8*3)+(7*1)+(6*5)+(5*5)+(4*6)+(3*7)+(2*6)+(1*7)=159
159 % 10 = 9
So 1315567-67-9 is a valid CAS Registry Number.

1315567-67-9Relevant articles and documents

Gateway synthesis of daphnane congeners and their protein kinase C affinities and cell-growth activities

Wender, Paul A.,Buschmann, Nicole,Cardin, Nathan B.,Jones, Lisa R.,Kan, Cindy,Kee, Jung-Min,Kowalski, John A.,Longcore, Kate E.

, p. 615 - 619 (2012/07/01)

The daphnane diterpene orthoesters constitute a structurally fascinating family of natural products that exhibit a remarkable range of potent biological activities. Although partial activity information is available for some natural daphnanes, little information exists for non-natural congeners or on how changes in structure affect mode of action, function, potency or selectivity. A gateway strategy designed to provide general synthetic access to natural and non-natural daphnanes is described and utilized in the synthesis of two novel members of this class. In this study, a commercially available tartrate derivative was elaborated through a key late-stage diversification intermediate into B-ring yuanhuapin analogues to initiate exploration of the structure-function relationships of this class. Protein kinase C was identified as a cellular target for these agents, and their activity against human lung and leukaemia cell lines was evaluated. The natural product and a novel non-natural analogue exhibited significant potency, but the epimeric epoxide was essentially inactive.

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