1199-46-8 | 2-Amino-4-tert-butylphenol

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$7.00	$5.00
25g	98%	in stock	$12.00	$9.00
100g	98%	in stock	$24.00	$17.00
500g	98%	in stock	$99.00	$69.00

Description

• Catalog Number: AA33313
• Chemical Name: 2-Amino-4-tert-butylphenol
• CAS Number: 1199-46-8
• Molecular Formula: C10H15NO
• Molecular Weight: 165.2322
• MDL Number: MFCD00007698
• SMILES: Oc1ccc(cc1N)C(C)(C)C
• NSC Number: 23803

Computed Properties

• Complexity: 150
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 2.5

Upstream Synthesis Route

2-Amino-4-(tert-butyl)phenol is a versatile chemical compound that finds wide applications in chemical synthesis processes. In organic chemistry, this compound serves as a key building block for the synthesis of various pharmaceuticals, dyes, and other specialty chemicals. Its unique molecular structure and reactivity make it a valuable intermediate in the production of diverse functional materials.2-Amino-4-(tert-butyl)phenol is commonly utilized as a precursor in the development of novel antioxidants due to its strong radical scavenging properties. It acts as a stabilizer in polymers and plastics, enhancing their durability and extending their lifespan. Furthermore, this compound is an essential ingredient in the synthesis of corrosion inhibitors, which are crucial in protecting metal surfaces from degradation.In the pharmaceutical industry, 2-Amino-4-(tert-butyl)phenol plays a vital role in the creation of various drugs and therapeutic agents. Its chemical functionality allows for the modification of molecular structures to enhance drug potency or efficacy. Moreover, this compound can be employed as a starting material for the synthesis of biologically active molecules with diverse pharmacological properties.Overall, the application of 2-Amino-4-(tert-butyl)phenol in chemical synthesis spans across multiple industries, contributing to the development of innovative products with enhanced performance and functionality.

Literature

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  Bioorganic & medicinal chemistry letters 20101101

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  Acta crystallographica. Section E, Structure reports online 20081201

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  The Journal of neuroscience : the official journal of the Society for Neuroscience 20080528

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  Biomeditsinskaia khimiia 20070101

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• Inhibition of peroxidase-catalyzed oxidation of 3,3 ,5,5 -tetramethylbenzidine by aminophenols.

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