5604-46-6 | 2-Amino-4,6-dichloropyrimidine-5-carbaldehyde

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$10.00	$7.00
5g	95%	in stock	$16.00	$11.00
10g	95%	in stock	$20.00	$14.00
25g	95%	in stock	$30.00	$21.00
100g	95%	in stock	$116.00	$82.00

Description

• Catalog Number: AI52571
• Chemical Name: 2-Amino-4,6-dichloropyrimidine-5-carbaldehyde
• CAS Number: 5604-46-6
• Molecular Formula: C5H3Cl2N3O
• Molecular Weight: 192.0028
• MDL Number: MFCD03001242
• SMILES: O=Cc1c(Cl)nc(nc1Cl)N
• NSC Number: 101680

Computed Properties

• Complexity: 145
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1.2

Upstream Synthesis Route

2-Amino-4,6-dichloro-5-pyrimidinecarbaldehyde is a highly versatile compound widely used in chemical synthesis. Its primary application lies in its role as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. In chemical synthesis, this compound serves as a crucial building block for the creation of complex molecules. Due to its unique structure and reactivity, 2-Amino-4,6-dichloro-5-pyrimidinecarbaldehyde is particularly valuable in the formation of heterocyclic compounds, which are prevalent in drug discovery and development. Furthermore, the presence of both amino and carbonyl functional groups in this compound enables it to participate in a variety of important chemical reactions, such as condensation, nucleophilic addition, and substitution reactions. These reactions allow for the modification and functionalization of the molecule, leading to the synthesis of novel compounds with diverse properties and applications.Overall, 2-Amino-4,6-dichloro-5-pyrimidinecarbaldehyde plays a critical role in advancing the field of chemical synthesis by enabling the efficient construction of complex molecules with potential therapeutic, agricultural, and industrial significance.

Literature

• Efficient microwave-assisted synthesis of 5-deazaflavine derivatives.

  Molecules (Basel, Switzerland) 20101020