Welcome to LookChem.com Sign In|Join Free
  • or
N-propylcyclohexanamine hydrochloride is an organic compound that serves as an intermediate in the synthesis of various pharmaceuticals. It is a derivative of cyclohexanamine with a propyl group attached to the nitrogen atom and a hydrochloride counterion, which contributes to its reactivity and utility in chemical reactions.

3592-82-3

Post Buying Request

3592-82-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

3592-82-3 Usage

Uses

Used in Pharmaceutical Synthesis:
N-propylcyclohexanamine hydrochloride is used as a key intermediate in the synthesis of (R)and (S)-rasagiline, which are important drugs for the treatment of Parkinson's disease. N-propylcyclohexanamine hydrochloride plays a crucial role in the reductive amination process, allowing for the selective formation of the desired enantiomers with high purity and yield.

Check Digit Verification of cas no

The CAS Registry Mumber 3592-82-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,9 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3592-82:
(6*3)+(5*5)+(4*9)+(3*2)+(2*8)+(1*2)=103
103 % 10 = 3
So 3592-82-3 is a valid CAS Registry Number.

3592-82-3Downstream Products

3592-82-3Relevant academic research and scientific papers

Direct Alkylation of Amines with Primary and Secondary Alcohols through Biocatalytic Hydrogen Borrowing

Montgomery, Sarah L.,Mangas-Sanchez, Juan,Thompson, Matthew P.,Aleku, Godwin A.,Dominguez, Beatriz,Turner, Nicholas J.

supporting information, p. 10491 - 10494 (2017/08/22)

The reductive aminase from Aspergillus oryzae (AspRedAm) was combined with a single alcohol dehydrogenase (either metagenomic ADH-150, an ADH from Sphingobium yanoikuyae (SyADH), or a variant of the ADH from Thermoanaerobacter ethanolicus (TeSADH W110A)) in a redox-neutral cascade for the biocatalytic alkylation of amines using primary and secondary alcohols. Aliphatic and aromatic secondary amines were obtained in up to 99 % conversion, as well as chiral amines directly from the racemic alcohol precursors in up to >97 % ee, releasing water as the only byproduct.

The N-Substitution of Aliphatic Primary Amines via 1-benzotriazoles: Preparation of Secondary Amines

Katritzky, Alan R.,Glen, Noble,Pilarski, Boguslaw,Harris, Philip

, p. 1443 - 1446 (2007/10/02)

A new method has been developed for the selective conversion of primary aliphatic amines into unsymmetrical secondary amines by Grignard reaction of 1-benzotriazoles 1.This method employs simple procedures and mild conditions, and is specific in that onyl monoalkylation of the primary amines results.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 3592-82-3