103030-28-0 | 6-Bromo-2-methylquinolin-4-ol

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$33.00	$23.00
5g	98%	in stock	$63.00	$45.00
10g	98%	in stock	$125.00	$88.00

Description

• Catalog Number: AD81028
• Chemical Name: 6-Bromo-2-methylquinolin-4-ol
• CAS Number: 103030-28-0
• Molecular Formula: C10H8BrNO
• Molecular Weight: 238.0806
• MDL Number: MFCD00484433
• SMILES: Brc1ccc2c(c1)c(O)cc(n2)C

Computed Properties

• Complexity: 262
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• XLogP3: 2.6

Upstream Synthesis Route

6-Bromo-2-methyl-4-quinolinol, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block and a key reagent in various reactions. This compound is widely used in the pharmaceutical and agrochemical industries for its unique structural features and diverse reactivity.One of the primary applications of 6-Bromo-2-methyl-4-quinolinol is in the synthesis of pharmaceutical compounds. Its bromine substituent and quinoline ring provide opportunities for functional group transformations, making it a valuable intermediate in the preparation of bioactive molecules. Additionally, the methyl group at position 2 enhances the compound's stability and influences the selectivity of reactions, leading to the efficient synthesis of target compounds.Furthermore, 6-Bromo-2-methyl-4-quinolinol is utilized in the development of novel agrochemicals due to its ability to undergo various synthetic transformations. By leveraging its unique structural properties, chemists can design and synthesize potent pesticides, herbicides, and fungicides with improved efficacy and selectivity. The presence of the bromine atom offers opportunities for further derivatization, allowing for the creation of a diverse range of agricultural chemicals.In summary, 6-Bromo-2-methyl-4-quinolinol serves as a valuable building block in chemical synthesis, enabling the creation of complex molecules with applications in pharmaceuticals and agrochemicals. Its versatile nature and reactivity make it a vital component in the development of innovative compounds for various industries.

Literature

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

  Bioorganic & medicinal chemistry letters 20101101

• 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