Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1083302-78-6

C23H24O8 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1083302-78-6 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1083302-78-6 Structure

  • Basic information

    1. Product Name: C23H24O8
    2. Synonyms: C23H24O8
    3. CAS NO:1083302-78-6
    4. Molecular Formula:
    5. Molecular Weight: 428.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1083302-78-6.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: C23H24O8(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H24O8(1083302-78-6)
    11. EPA Substance Registry System: C23H24O8(1083302-78-6)

  • 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: 1083302-78-6(Hazardous Substances Data)

1083302-78-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1083302-78-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,3,3,0 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1083302-78:
(9*1)+(8*0)+(7*8)+(6*3)+(5*3)+(4*0)+(3*2)+(2*7)+(1*8)=126
126 % 10 = 6
So 1083302-78-6 is a valid CAS Registry Number.

1083302-78-6Upstream product

1083302-78-6Relevant articles and documents

Concise stereoselective synthesis of (-)-podophyllotoxin by an intermolecular iron(III)-catalyzed Friedel-Crafts alkylation

Stadler, Daniel,Bach, Thorsten

supporting information; scheme or table, p. 7557 - 7559 (2009/03/12)

(Chemical Equation Presented) Without further ado, the building blocks 1-3 were combined in three C-C bond-forming reactions to provide the enantiomerically pure natural product (-)-podophyllotoxin (4). The stereogenic center at C1 was generated in the key reaction, a diastereoselective iron(III)-catalyzed intermolecular Friedel-Crafts alkylation.

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 1083302-78-6