199177-26-9 | 3-Bromo-5-hydroxybenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$7.00	$5.00
250mg	98%	in stock	$11.00	$8.00
1g	98%	in stock	$18.00	$13.00
10g	98%	in stock	$139.00	$98.00
25g	98%	in stock	$329.00	$230.00

Description

• Catalog Number: AB08588
• Chemical Name: 3-Bromo-5-hydroxybenzaldehyde
• CAS Number: 199177-26-9
• Molecular Formula: C7H5BrO2
• Molecular Weight: 201.0174
• MDL Number: MFCD06797981
• SMILES: O=Cc1cc(O)cc(c1)Br

Computed Properties

• Complexity: 127
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1.7

Upstream Synthesis Route

Benzaldehyde, 3-bromo-5-hydroxy-, is a powerful tool in chemical synthesis due to its unique properties and versatile applications. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its presence allows for the introduction of both bromine and hydroxyl functional groups into organic molecules with precision, enabling the synthesis of complex structures that would be otherwise challenging to achieve.In organic chemistry, the 3-bromo-5-hydroxy-benzaldehyde can be utilized as a key intermediate in the construction of biologically active compounds, particularly in the development of pharmaceuticals for medicinal purposes. Its distinct reactivity and compatibility with a wide range of substrates make it an ideal reagent for carrying out important transformations such as nucleophilic substitution, cross-coupling reactions, and cyclization processes. By incorporating this compound into synthetic pathways, chemists can access a diverse array of molecules with enhanced potency and desirable pharmacological properties.Furthermore, the strategic incorporation of benzaldehyde, 3-bromo-5-hydroxy-, in chemical synthesis enables researchers to tailor the structure and function of target compounds for specific applications. Its ability to serve as a directing group in various synthetic methodologies allows for precise control over regioselectivity and stereoselectivity, leading to the efficient construction of complex molecular architectures. This compound's versatility and reactivity open up a realm of possibilities for designing novel chemical entities and advancing the frontier of organic synthesis.In summary, the application of benzaldehyde, 3-bromo-5-hydroxy-, in chemical synthesis offers a wealth of opportunities for organic chemists to explore new synthetic pathways, expand the scope of chemical reactions, and create valuable compounds with diverse functionalities. Its role as a valuable building block and versatile reagent underscores its significance in driving innovation and discovery in the field of chemistry.