4318-37-0 | N-Methylhomopiperazine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$10.00	$7.00
5g	98%	in stock	$21.00	$15.00
10g	98%	in stock	$40.00	$28.00
25g	98%	in stock	$99.00	$70.00

Description

• Catalog Number: AB49393
• Chemical Name: N-Methylhomopiperazine
• CAS Number: 4318-37-0
• Molecular Formula: C6H14N2
• Molecular Weight: 114.1888
• MDL Number: MFCD00059810
• SMILES: CN1CCNCCC1
• NSC Number: 21211

Computed Properties

• Complexity: 63.5
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• XLogP3: -0.4

Upstream Synthesis Route

N-Methylhomopiperazine is a versatile compound commonly used in chemical synthesis as a building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique molecular structure and reactivity make it an essential reagent in organic chemistry.In chemical synthesis, N-Methylhomopiperazine serves as a key intermediate in the synthesis of diverse organic molecules due to its ability to participate in a wide range of reactions. Its nitrogen-containing heterocyclic ring provides a stable framework for the attachment of different functional groups, allowing chemists to tailor its chemical properties for specific applications.One important application of N-Methylhomopiperazine is in the synthesis of bioactive molecules such as pharmaceutical drugs and medicinal compounds. By incorporating N-Methylhomopiperazine into the molecular structure of a drug candidate, researchers can enhance its biological activity, solubility, and pharmacokinetic properties, leading to the development of more effective and target-specific medications.Additionally, N-Methylhomopiperazine is utilized in the synthesis of agrochemicals, dyes, and other specialty chemicals where its unique properties play a crucial role in the design and production of high-performance products for various industries. Its versatility and compatibility with a wide range of chemical reactions make it a valuable tool for synthetic chemists seeking to create innovative compounds with specific functionalities and applications.

Literature

• Faster oxygen atom transfer catalysis with a tungsten dioxo complex than with its molybdenum analog.

  Dalton transactions (Cambridge, England : 2003) 20110821

• Spectral, electrochemical and molecular orbital studies on solvatochromic mixed ligand copper(II) complexes of malonate and diamine derivatives.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20030401