7752-82-1 | 2-Amino-5-bromopyrimidine

Packsize	Purity	Availability	Price	Discounted Price
10g	98%	in stock	$8.00	$5.00
25g	98%	in stock	$12.00	$9.00
100g	98%	in stock	$31.00	$22.00

Description

• Catalog Number: AB43786
• Chemical Name: 2-Amino-5-bromopyrimidine
• CAS Number: 7752-82-1
• Molecular Formula: C4H4BrN3
• Molecular Weight: 173.9987
• MDL Number: MFCD00012341
• SMILES: Brc1cnc(nc1)N
• NSC Number: 27269

Computed Properties

• Complexity: 69.7
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• XLogP3: 0.5

Upstream Synthesis Route

2-Amino-5-Bromopyrimidine is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a key building block in the development of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 2-Amino-5-Bromopyrimidine is often employed as a key intermediate in the preparation of heterocyclic compounds. Its ability to undergo various substitution reactions makes it a valuable precursor in the synthesis of complex molecules. Additionally, the amino group present in this compound allows for further functionalization, enabling the introduction of different substituents to modulate the properties of the final product.One of the notable applications of 2-Amino-5-Bromopyrimidine is its use in the synthesis of pharmaceutical compounds. By incorporating this building block into drug molecules, chemists can target specific biological pathways or interactions, leading to the development of new therapeutic agents. Furthermore, its role in agrochemical synthesis contributes to the production of effective pesticides and herbicides used in crop protection.Overall, 2-Amino-5-Bromopyrimidine plays a crucial role in chemical synthesis, facilitating the creation of diverse molecules with significant applications in various industries. Its versatility and reactivity make it a valuable component in the toolbox of synthetic chemists aiming to design novel compounds for a range of purposes.

Literature

• Synthesis of pyridine, pyrimidine and pyridinone C-nucleoside phosphoramidites for probing cytosine function in RNA.

  The Journal of organic chemistry 20091106