Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1401412-99-4

N-(1-cyclohexyl-2-phenylethyl)cyclohexanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1401412-99-4 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1401412-99-4 Structure

  • Basic information

    1. Product Name: N-(1-cyclohexyl-2-phenylethyl)cyclohexanamine
    2. Synonyms: N-(1-cyclohexyl-2-phenylethyl)cyclohexanamine
    3. CAS NO:1401412-99-4
    4. Molecular Formula:
    5. Molecular Weight: 285.473
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1401412-99-4.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-(1-cyclohexyl-2-phenylethyl)cyclohexanamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(1-cyclohexyl-2-phenylethyl)cyclohexanamine(1401412-99-4)
    11. EPA Substance Registry System: N-(1-cyclohexyl-2-phenylethyl)cyclohexanamine(1401412-99-4)

  • 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: 1401412-99-4(Hazardous Substances Data)

1401412-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1401412-99-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,4,1 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1401412-99:
(9*1)+(8*4)+(7*0)+(6*1)+(5*4)+(4*1)+(3*2)+(2*9)+(1*9)=104
104 % 10 = 4
So 1401412-99-4 is a valid CAS Registry Number.

1401412-99-4Downstream Products

1401412-99-4Relevant articles and documents

A general method for the one-pot reductive functionalization of secondary amides

Huang, Pei-Qiang,Huang, Ying-Hong,Xiao, Kai-Jiong,Wang, Yu,Xia, Xiao-Er

, p. 2861 - 2868 (2015)

A one-pot reaction for the transformation of common secondary amides into amines with C-C bond formation is described. This method consists of in situ amide activation with Tf2O-partial reduction-addition of C-nucleophiles. The method is general in scope, which allows employing both hard nucleophiles (RMgX, RLi) and soft nucleophiles, as well as enolates. With the use of soft nucleophiles, the reaction proceeded with high chemoselectivity at a secondary amide in the presence of ester, cyano, nitro, and tertiary amide groups.

Direct transformation of secondary amides into secondary amines: Triflic anhydride activated reductive alkylation

Xiao, Kai-Jiong,Wang, Ai-E,Huang, Pei-Qiang

supporting information; experimental part, p. 8314 - 8317 (2012/09/08)

Versatile and mild: The first general method for the title transformation has been developed (see scheme; 2-F-Py=2-fluoropyridine; Tf=trifluorosulfonyl). The amines are synthesized in good yields and the ketimine intermediates can be isolated before the r

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 1401412-99-4