Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1338672-83-5

C16H22O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1338672-83-5 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1338672-83-5 Structure

  • Basic information

    1. Product Name: C16H22O3S
    2. Synonyms: C16H22O3S
    3. CAS NO:1338672-83-5
    4. Molecular Formula:
    5. Molecular Weight: 294.415
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1338672-83-5.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: C16H22O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H22O3S(1338672-83-5)
    11. EPA Substance Registry System: C16H22O3S(1338672-83-5)

  • 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: 1338672-83-5(Hazardous Substances Data)

1338672-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1338672-83-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,6,7 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1338672-83:
(9*1)+(8*3)+(7*3)+(6*8)+(5*6)+(4*7)+(3*2)+(2*8)+(1*3)=185
185 % 10 = 5
So 1338672-83-5 is a valid CAS Registry Number.

1338672-83-5Downstream Products

1338672-83-5Relevant articles and documents

Regioselective radical bromoallylation of allenes leading to 2-bromo-substituted 1,5-dienes

Kippo, Takashi,Fukuyama, Takahide,Ryu, Ilhyong

, p. 3864 - 3867 (2011/09/15)

The regioselective radical bromoallylation of allenes proceeded efficiently in the presence of AIBN as a radical initiator to give 2-bromo-substituted 1,5-dienes in excellent yields. The addition of a bromine radical took place regioselectively onto the central carbon of allenes generating a stable allyl radical, which underwent addition/β-fragmentation reactions with allylbromides. The products could be further functionalized by Pd-catalyzed coupling reactions.

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 1338672-83-5