Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1521267-00-4

C18H36O3Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1521267-00-4 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1521267-00-4 Structure

  • Basic information

    1. Product Name: C18H36O3Si
    2. Synonyms: C18H36O3Si
    3. CAS NO:1521267-00-4
    4. Molecular Formula:
    5. Molecular Weight: 328.568
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1521267-00-4.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: C18H36O3Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H36O3Si(1521267-00-4)
    11. EPA Substance Registry System: C18H36O3Si(1521267-00-4)

  • 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: 1521267-00-4(Hazardous Substances Data)

1521267-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1521267-00-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,2,1,2,6 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1521267-00:
(9*1)+(8*5)+(7*2)+(6*1)+(5*2)+(4*6)+(3*7)+(2*0)+(1*0)=124
124 % 10 = 4
So 1521267-00-4 is a valid CAS Registry Number.

1521267-00-4Relevant articles and documents

A concise synthesis of (-)-lasonolide A

Trost, Barry M.,Stivala, Craig E.,Hull, Kami L.,Huang, Audris,Fandrick, Daniel R.

, p. 88 - 91 (2014)

Lasonolide A is a novel polyketide displaying potent anticancer activity across a broad range of cancer cell lines. Here, an enantioselective convergent total synthesis of the (-)-lasonolide A in 16 longest linear and 34 total steps is described. This approach significantly reduces the step count compared to other known syntheses. The synthetic strategy utilizes alkyne-bearing substrates as core building blocks and is highlighted by stitching together two similarly complex halves via a key Ru-catalyzed alkene-alkyne coupling and macrolactionization.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1521267-00-4