Welcome to LookChem.com Sign In|Join Free

CAS

  • or

544459-32-7

3-cyclohexyl-N-(2-pyridinyl)propanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

544459-32-7 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 544459-32-7 Structure

  • Basic information

    1. Product Name: 3-cyclohexyl-N-(2-pyridinyl)propanamide
    2. Synonyms: 3-cyclohexyl-N-(2-pyridinyl)propanamide
    3. CAS NO:544459-32-7
    4. Molecular Formula: C14H20N2O
    5. Molecular Weight: 232.3214
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 544459-32-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-cyclohexyl-N-(2-pyridinyl)propanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-cyclohexyl-N-(2-pyridinyl)propanamide(544459-32-7)
    11. EPA Substance Registry System: 3-cyclohexyl-N-(2-pyridinyl)propanamide(544459-32-7)

  • 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: 544459-32-7(Hazardous Substances Data)

544459-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 544459-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,4,4,5 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 544459-32:
(8*5)+(7*4)+(6*4)+(5*4)+(4*5)+(3*9)+(2*3)+(1*2)=167
167 % 10 = 7
So 544459-32-7 is a valid CAS Registry Number.

544459-32-7Downstream Products

544459-32-7Relevant articles and documents

Ru-catalyzed hydroamidation of alkenes and cooperative aminocarboxylation procedure with chelating formamide

Ko, Sangwon,Han, Hoon,Chang, Sukbok

, p. 2687 - 2690 (2007/10/03)

(Matrix presented) A strategy of chelation-assisted activation of formamide was employed to achieve hydroamidation of alkenes to generate one-carbon-elongated amides in moderate to good selectivity and yields. Also reported is the two-metal-catalyzed cooperative aminocarboxylation of aryl iodides, in which Ru is presumed to catalyze decarbonylation of formamide to release carbon monoxide and amine for the subsequent Pd-catalyzed aminocarboxylation routes, thus enabling the net transformation to be performed in the absence of external CO pressure.

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 544459-32-7