104-23-4 | 4'-Aminoazobenzene-4-sulphonic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$25.00	$18.00
5g	95%	in stock	$63.00	$45.00
25g	95%	in stock	$231.00	$162.00
100g	95%	in stock	$692.00	$484.00

Description

• Catalog Number: AD70949
• Chemical Name: 4'-Aminoazobenzene-4-sulphonic acid
• CAS Number: 104-23-4
• Molecular Formula: C12H11N3O3S
• Molecular Weight: 277.299
• MDL Number: MFCD00035564
• SMILES: Nc1ccc(cc1)/N=N/c1ccc(cc1)S(=O)(=O)O
• NSC Number: 4704

Computed Properties

• Complexity: 402
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 6
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• XLogP3: 2.2

Upstream Synthesis Route

4-((4-aminophenyl)diazenyl)benzenesulfonic acid, commonly known as $name$, is a versatile chemical compound used in various chemical synthesis reactions. This compound is often employed as a diazo dye intermediate, where its unique structure allows for the formation of vibrant and stable azo dyes. In chemical synthesis, $name$ serves as a crucial building block for the creation of azo compounds, which find wide applications in industries such as textiles, cosmetics, and food coloring.Aside from its role in dye synthesis, 4-((4-aminophenyl)diazenyl)benzenesulfonic acid is also utilized as a reagent in organic transformations. Its reactive amino and diazo groups enable it to participate in coupling reactions, forming carbon-carbon or carbon-nitrogen bonds to create structurally diverse molecules. Moreover, due to its sulfonic acid moiety, $name$ can act as a catalyst in certain organic reactions, facilitating the conversion of substrates to desired products efficiently.Overall, the use of 4-((4-aminophenyl)diazenyl)benzenesulfonic acid in chemical synthesis highlights its significance in enabling the creation of functionalized compounds with diverse applications in various industrial and research settings.

Literature

• Assay of the pyruvate dehydrogenase complex by coupling with recombinant chicken liver arylamine N-acetyltransferase.

  Analytical biochemistry 20060901