Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1311296-21-5

(+)-[(4R)-4-ethyl-5-hexen-1-yl]benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1311296-21-5 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1311296-21-5 Structure

  • Basic information

    1. Product Name: (+)-[(4R)-4-ethyl-5-hexen-1-yl]benzene
    2. Synonyms: (+)-[(4R)-4-ethyl-5-hexen-1-yl]benzene
    3. CAS NO:1311296-21-5
    4. Molecular Formula:
    5. Molecular Weight: 188.313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1311296-21-5.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: (+)-[(4R)-4-ethyl-5-hexen-1-yl]benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+)-[(4R)-4-ethyl-5-hexen-1-yl]benzene(1311296-21-5)
    11. EPA Substance Registry System: (+)-[(4R)-4-ethyl-5-hexen-1-yl]benzene(1311296-21-5)

  • 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: 1311296-21-5(Hazardous Substances Data)

1311296-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1311296-21-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,1,2,9 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1311296-21:
(9*1)+(8*3)+(7*1)+(6*1)+(5*2)+(4*9)+(3*6)+(2*2)+(1*1)=115
115 % 10 = 5
So 1311296-21-5 is a valid CAS Registry Number.

1311296-21-5Relevant articles and documents

Catalyst control in sequential asymmetric allylic substitution: Stereodivergent access to N,N-diprotected unnatural amino acids

Tosatti, Paolo,Campbell, Amanda J.,House, David,Nelson, Adam,Marsden, Stephen P.

experimental part, p. 5495 - 5501 (2011/09/19)

The sequential use of Cu-catalyzed asymmetric allylic alkylation, olefin cross-metathesis, and Ir-catalyzed asymmetric allylic amination allows the concise, stereodivergent synthesis of complex chiral amines with complete regiocontrol and good diastereose

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 1311296-21-5