109-82-0 | Methylenaminoacetonitrile

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$25.00	$18.00
25g	98%	in stock	$31.00	$22.00
500g	98%	in stock	$289.00	$202.00

Description

• Catalog Number: AB76190
• Chemical Name: Methylenaminoacetonitrile
• CAS Number: 109-82-0
• Molecular Formula: C3H6N2O
• Molecular Weight: 86.0925
• MDL Number: MFCD00001889
• SMILES: NC(=O)CN=C

Computed Properties

• Complexity: 66.2
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 5
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 1.3

Upstream Synthesis Route

Methyleneaminoacetonitrile is a valuable compound commonly employed in chemical synthesis processes. It serves as a crucial intermediate in the production of various organic compounds due to its versatile reactivity and structural features. In the realm of chemical synthesis, Methyleneaminoacetonitrile plays a significant role as a key building block in the creation of a wide range of compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its chemical structure contains functional groups that facilitate diverse transformations, making it a versatile and sought-after molecule in the synthesis of complex organic substances.One prominent application of Methyleneaminoacetonitrile is in the synthesis of amino acids. By reacting with appropriate reagents and undergoing specific chemical reactions, it can be transformed into various amino acid derivatives, which are essential components in the production of proteins, peptides, and other biologically active molecules.Furthermore, Methyleneaminoacetonitrile can be utilized in the preparation of heterocyclic compounds, which are widely used in medicinal chemistry and materials science. Its reactivity allows for the incorporation of nitrogen-containing rings into organic molecules, expanding the structural diversity and potential applications of the resulting compounds.Overall, Methyleneaminoacetonitrile serves as a versatile and indispensable tool in chemical synthesis, enabling the creation of diverse organic compounds with applications across various industries.

Literature

• Evaluation of dose-response curve analysis in delineating shared or different molecular sites of action for osteolathyrogens.

  Environmental toxicology and pharmacology 20040301