Welcome to LookChem.com Sign In|Join Free

CAS

  • or

137452-05-2

N-Benzyl-2-(p-tolylsulphinyl)propylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137452-05-2 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 137452-05-2 Structure

  • Basic information

    1. Product Name: N-Benzyl-2-(p-tolylsulphinyl)propylamine
    2. Synonyms:
    3. CAS NO:137452-05-2
    4. Molecular Formula:
    5. Molecular Weight: 287.426
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 137452-05-2.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: N-Benzyl-2-(p-tolylsulphinyl)propylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Benzyl-2-(p-tolylsulphinyl)propylamine(137452-05-2)
    11. EPA Substance Registry System: N-Benzyl-2-(p-tolylsulphinyl)propylamine(137452-05-2)

  • 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: 137452-05-2(Hazardous Substances Data)

137452-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137452-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,5 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 137452-05:
(8*1)+(7*3)+(6*7)+(5*4)+(4*5)+(3*2)+(2*0)+(1*5)=122
122 % 10 = 2
So 137452-05-2 is a valid CAS Registry Number.

137452-05-2Downstream Products

137452-05-2Relevant articles and documents

Stereoselective Protonation and Reduction of β-Sulphinyl Enamines. X-Ray Molecular Structure of N-Benzyl-2-(p-tolylsulphinyl)propylamine

Kawecki, Robert,Kozerski, Lech,Urbanczyk-Lipkowska, Zofia,Bocelli, Gabriele

, p. 2255 - 2260 (2007/10/02)

Reduction of β-substituted β-sulphinyl enamines by acyloxyborohydrides in the presence of carboxylic acids leads to β-sulphinyl amines in good chemical yield and diastereoisomeric excess (de) up to 92percent.Two methods of reduction, differing by the introduction sequence of the acid, are examined.The stereoselectivity is enhanced with large proton donors and strong acids but is less dependent on the type of reducing agent and solvent used.A mechanism for the stereoselective protonation is proposed.

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 137452-05-2