1187-42-4 | Diaminomaleonitrile

Packsize	Purity	Availability	Price	Discounted Price
5g	96%	in stock	$6.00	$4.00
25g	96%	in stock	$14.00	$10.00
500g	96%	in stock	$247.00	$173.00

Description

• Catalog Number: AB43563
• Chemical Name: Diaminomaleonitrile
• CAS Number: 1187-42-4
• Molecular Formula: C4H4N4
• Molecular Weight: 108.1014
• MDL Number: MFCD00001870
• SMILES: N#C/C(=C(C#N)/N)/N
• NSC Number: 266758

Computed Properties

• Complexity: 183
• Covalently-Bonded Unit Count: 1
• Defined Bond Stereocenter Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• XLogP3: -1

Upstream Synthesis Route

2,3-Diaminomaleonitrile is widely used in chemical synthesis as a versatile building block in the production of various compounds. Due to its unique structure and reactivity, this compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials with diverse applications.One of the main applications of 2,3-Diaminomaleonitrile is its role in the synthesis of heterocyclic compounds such as pyrroles, pyrimidines, and pyridazines. These heterocycles are essential components in the development of drugs and bioactive molecules with therapeutic properties. By utilizing 2,3-Diaminomaleonitrile as a starting material, chemists can efficiently access these important heterocycles through various synthetic routes.Furthermore, 2,3-Diaminomaleonitrile is employed in the preparation of functionalized compounds with nitrogen-containing motifs. The presence of amino groups in the molecule allows for further derivatization, enabling the introduction of specific functional groups for tailored properties or enhanced reactivity. This versatility makes 2,3-Diaminomaleonitrile a valuable tool in the design and synthesis of advanced materials for various industrial applications.In summary, the application of 2,3-Diaminomaleonitrile in chemical synthesis offers a wide range of possibilities for the creation of complex molecules with significant biological and material properties. Its importance as a key intermediate underscores its value in advancing the field of organic chemistry and addressing challenges in drug discovery, materials science, and other innovative areas of research.

Literature

• Conformational and vibrational studies of isomeric hydrogen cyanide tetramers by quantum chemical methods.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20120401

• New insights into the characterization of 'insoluble black HCN polymers'.

  Chemistry & biodiversity 20120101

• HCN polymers characterized by SSNMR: solid state reaction of crystalline tetramer (diaminomaleonitrile).

  The Journal of chemical physics 20090407

• A novel synthesis of highly substituted imidazo[1,5-a]pyrazine derivatives by 3-CR/2-CR sequence.

  Molecular diversity 20090201

• Revisiting the reaction between diaminomaleonitrile and aromatic aldehydes: a green chemistry approach.

  Molecules (Basel, Switzerland) 20061111

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501