Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1333378-30-5

C36H39N7O6S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1333378-30-5 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1333378-30-5 Structure

  • Basic information

    1. Product Name: C36H39N7O6S2
    2. Synonyms: C36H39N7O6S2
    3. CAS NO:1333378-30-5
    4. Molecular Formula:
    5. Molecular Weight: 729.881
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1333378-30-5.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: C36H39N7O6S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C36H39N7O6S2(1333378-30-5)
    11. EPA Substance Registry System: C36H39N7O6S2(1333378-30-5)

  • 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: 1333378-30-5(Hazardous Substances Data)

1333378-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1333378-30-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,3,7 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1333378-30:
(9*1)+(8*3)+(7*3)+(6*3)+(5*3)+(4*7)+(3*8)+(2*3)+(1*0)=145
145 % 10 = 5
So 1333378-30-5 is a valid CAS Registry Number.

1333378-30-5Relevant articles and documents

Synthetic studies on dragmacidin D: Synthesis and assembly of three fragments towards an advanced intermediate

Oikawa, Masato,Ikoma, Minoru,Sasaki, Makoto

, p. 4654 - 4666 (2011/10/03)

We report herein the approach to the key advanced intermediate in the synthesis of the bioactive marine natural product dragmacidin D. By employing a modular synthesis strategy of three fragments (5, 7, and 8), the advanced intermediate 3 has been successfully synthesized in 2.5% yield over 15 steps by starting from nitrotoluene 20. The synthesis also involves sequential cross-coupling reactions, namely Sonogashira and Suzuki-Miyaura reactions, so that various analogues can be efficiently synthesized, which will allow the study of structure-activity relationships of dragmacidin D.

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 1333378-30-5