14381-51-2 | 3-Bromocatechol

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$6.00	$4.00
5g	97%	in stock	$12.00	$9.00
10g	95%	in stock	$21.00	$15.00
15g	95%	in stock	$27.00	$19.00
25g	95%	in stock	$44.00	$31.00
50g	95%	in stock	$85.00	$60.00
100g	95%	in stock	$166.00	$116.00
250g	95%	in stock	$411.00	$288.00
500g	95%	in stock	$713.00	$499.00

Description

• Catalog Number: AA70326
• Chemical Name: 3-Bromocatechol
• CAS Number: 14381-51-2
• Molecular Formula: C6H5BrO2
• Molecular Weight: 189.0067
• MDL Number: MFCD00869768
• SMILES: Oc1c(O)cccc1Br

Computed Properties

• Complexity: 97.1
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• XLogP3: 2.3

Upstream Synthesis Route

$Name$ is a versatile compound that finds wide application in chemical synthesis. Its key role lies in its function as a precursor in the synthesis of various organic compounds. Specifically, 3-Bromocatechol is commonly used as a building block in the creation of complex molecules due to its unique reactivity and properties.One major application of 3-Bromocatechol is in the synthesis of pharmaceuticals, where it serves as a crucial intermediate in the production of active pharmaceutical ingredients. Its ability to undergo various chemical reactions makes it a valuable tool for chemists in designing and developing new drugs with specific biological activities.Additionally, 3-Bromocatechol is employed in the synthesis of agrochemicals and specialty chemicals. By using this compound as a starting material, chemists can access a wide range of structurally diverse molecules that have applications in crop protection, materials science, and other industries.In the field of organic chemistry, 3-Bromocatechol plays a vital role in the construction of complex molecular frameworks through various synthetic methods such as cross-coupling reactions, substitution reactions, and cascade reactions. Its versatility and reactivity make it a valuable asset in the hands of synthetic chemists seeking to create novel compounds with unique properties.

Literature

• Substrate specificity of Sphingobium chlorophenolicum 2,6-dichlorohydroquinone 1,2-dioxygenase.

  Biochemistry 20111018

• Measurement of polybrominated diphenyl ethers and metabolites in mouse plasma after exposure to a commercial pentabromodiphenyl ether mixture.

  Environmental health perspectives 20070701

• Site-specific arylation of rat glutathione s-transferase A1 and A2 by bromobenzene metabolites in vivo.

  Chemical research in toxicology 20061101

• Alpha-(N-carbamoyl)alkylcuprate chemistry in the synthesis of nitrogen heterocycles.

  The Journal of organic chemistry 20020208