121-88-0 | 2-Amino-5-nitrophenol

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$15.00	$10.00
5g	97%	in stock	$16.00	$11.00
25g	97%	in stock	$30.00	$21.00
100g	97%	in stock	$90.00	$63.00
500g	97%	in stock	$323.00	$226.00

Description

• Catalog Number: AD32144
• Chemical Name: 2-Amino-5-nitrophenol
• CAS Number: 121-88-0
• Molecular Formula: C6H6N2O3
• Molecular Weight: 154.1234
• MDL Number: MFCD00007692
• SMILES: [O-][N+](=O)c1ccc(c(c1)O)N
• NSC Number: 7087

Computed Properties

• Complexity: 156
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• XLogP3: 1.5

Upstream Synthesis Route

2-Amino-5-nitrophenol, also known as 5-Nitro-o-aminophenol, is a key chemical compound widely used in chemical synthesis processes. This versatile intermediate plays a crucial role in the production of various organic compounds and pigments due to its unique properties and reactivity. In chemical synthesis, 2-Amino-5-nitrophenol serves as a valuable building block for the synthesis of dyes, pharmaceuticals, agrochemicals, and other specialty chemicals. Its functional groups allow for various derivatization reactions, making it a valuable tool for creating complex molecular structures. Additionally, 2-Amino-5-nitrophenol can be employed as a catalyst or a reagent in different synthetic pathways, enabling chemists to access a wide range of target molecules efficiently. Overall, the utilization of 2-Amino-5-nitrophenol in chemical synthesis highlights its significance as a versatile and indispensable component in the realm of organic chemistry.

Literature

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  PloS one 20120101

• 2-Hy-droxy-N-(4-meth-oxy-benz-yl)-4-nitro-anilinium chloride.

  Acta crystallographica. Section E, Structure reports online 20110801

• anticonvulsant and toxicity evaluation of newer 4H-benzo[1,4]oxazin-3-ones: The effect of two hydrogen bonding domains.

  Archiv der Pharmazie 20101101

• Inter-laboratory evaluation of the bioluminescent Salmonella reverse mutation assay using 10 model chemicals.

  Mutagenesis 20090901

• Final report on the safety assessment of amino nitrophenols as used in hair dyes.

  International journal of toxicology 20090101

• Synthesis of novel 7-benzylamino-2H-1,4-benzoxazin-3(4H)-ones as anticonvulsant agents.

  European journal of medicinal chemistry 20080601

• An animal model assessment of common dye-induced allergic contact dermatitis.

  Journal of cosmetic science 20070101

• Separation and determination of nitrobenzenes by micellar electrokinetic chromatography and high-performance liquid chromatography.

  Journal of chromatography. A 20021206