619-19-2 | 2-Hydroxy-4-nitrobenzoic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$15.00	$10.00
1g	95%	in stock	$16.00	$11.00
5g	95%	in stock	$33.00	$23.00
25g	95%	in stock	$86.00	$60.00
100g	95%	in stock	$315.00	$221.00
500g	95%	in stock	$1,465.00	$1,025.00

Description

• Catalog Number: AG64338
• Chemical Name: 2-Hydroxy-4-nitrobenzoic acid
• CAS Number: 619-19-2
• Molecular Formula: C7H5NO5
• Molecular Weight: 183.1183
• MDL Number: MFCD00071505
• SMILES: OC(=O)c1ccc(cc1O)[N+](=O)[O-]
• NSC Number: 882

Computed Properties

• Complexity: 223
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 2.3

Upstream Synthesis Route

2-Hydroxy-4-nitrobenzoic acid, also known as Salicylic acid-4-nitro or SNBSA, is a versatile compound widely utilized in chemical synthesis. This chemical compound plays a crucial role as a starting material in the synthesis of various pharmaceuticals, dyes, and organic compounds.One of the key applications of 2-Hydroxy-4-nitrobenzoic acid is in the synthesis of salicylanilide, a compound commonly used as an antimicrobial agent in pharmaceuticals. The reaction involves the condensation of 2-Hydroxy-4-nitrobenzoic acid with aniline under specific reaction conditions to yield salicylanilide.Furthermore, 2-Hydroxy-4-nitrobenzoic acid is utilized in the synthesis of azo dyes, which find applications in the textile industry. By coupling 2-Hydroxy-4-nitrobenzoic acid with various diazonium salts, a range of colorful azo dyes can be produced through diazo coupling reactions.Additionally, this compound can be employed as a building block in the preparation of other organic compounds due to its functional groups and reactivity. Its ability to undergo various chemical transformations makes it a valuable intermediate in the synthesis of complex organic molecules.In conclusion, 2-Hydroxy-4-nitrobenzoic acid serves as a fundamental building block in chemical synthesis, enabling the production of a diverse range of compounds with important industrial applications.

Literature

• catena-Poly[[[diaqua-cobalt(II)]-μ-(3,5-dinitro-2-oxidobenzoato)-κO,O:O-[tetra-aqua-cobalt(II)]-μ-(3,5-dinitro-2-oxidobenzoato)-κO:O,O] dihydrate].

  Acta crystallographica. Section E, Structure reports online 20110101