5399-92-8 | 4-Chloro-1H-pyrazolo[3,4-d]pyrimidine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$10.00	$7.00
5g	95%	in stock	$17.00	$12.00

Description

• Catalog Number: AB44916
• Chemical Name: 4-Chloro-1H-pyrazolo[3,4-d]pyrimidine
• CAS Number: 5399-92-8
• Molecular Formula: C5H3ClN4
• Molecular Weight: 154.5571
• MDL Number: MFCD03030404
• SMILES: Clc1ncnc2c1cn[nH]2
• NSC Number: 4937

Computed Properties

• Complexity: 131
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• XLogP3: 1.1

Upstream Synthesis Route

4-Chloro-1H-pyrazolo[3,4-d]pyrimidine, also known as $name$, is a versatile building block widely utilized in chemical synthesis. This compound plays a crucial role in the development of various pharmaceuticals, agrochemicals, and materials due to its unique chemical properties.In organic synthesis, 4-Chloro-1H-pyrazolo[3,4-d]pyrimidine serves as a key intermediate for the construction of complex molecules. Its reactivity allows for the creation of diverse molecular structures through functional group transformations, such as nucleophilic substitution, cross-coupling reactions, and cyclization processes.One of the prominent applications of 4-Chloro-1H-pyrazolo[3,4-d]pyrimidine is in the synthesis of bioactive compounds and pharmaceuticals. By incorporating this compound into different synthetic routes, chemists can access novel drug candidates with potential therapeutic properties. Additionally, its compatibility with various reaction conditions and functional group manipulations make it a valuable tool for medicinal chemistry research.Furthermore, 4-Chloro-1H-pyrazolo[3,4-d]pyrimidine is also utilized in the development of agrochemical products. Its structural features enable the modification of pesticide and herbicide molecules, enhancing their efficacy and selectivity in agricultural applications. By leveraging the synthetic utility of this compound, chemists can tailor agrochemical formulations to improve crop protection and yield.Overall, the strategic use of 4-Chloro-1H-pyrazolo[3,4-d]pyrimidine in chemical synthesis enables the creation of diverse molecular scaffolds with applications ranging from pharmaceuticals to agrochemicals. Its versatility and synthetic accessibility make it a valuable building block for designing innovative molecules with potential benefits in various industries.

Literature

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101