850085-99-3

Basic information

• Product Name: 5-Amino-2-isopropylphenol
• Synonyms: 5-Amino-2-isopropylphenol
• CAS NO: 850085-99-3
• Molecular Formula: C₉H₁₃NO
• Molecular Weight: 151.20562
• EINECS: -0
• Mol File: 850085-99-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-Amino-2-isopropylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Amino-2-isopropylphenol(850085-99-3)
• EPA Substance Registry System: 5-Amino-2-isopropylphenol(850085-99-3)

Safety Data

• Hazardous Substances Data: 850085-99-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
5-Amino-2-isopropylphenol is used as an intermediate in the production of pharmaceuticals for its ability to contribute to the synthesis of various organic compounds, enhancing the development of new medications.
Used in Cosmetics Industry:
In the cosmetics industry, 5-Amino-2-isopropylphenol is utilized as a key component in the formulation of cosmetic products, leveraging its chemical properties to improve product efficacy and quality.
Used in Organic Synthesis:
5-Amino-2-isopropylphenol serves as an intermediate in the synthesis of a range of organic compounds, playing a crucial role in the creation of diverse chemical products.

Upstream product

• 643-28-7 2-isopropylaniline 
• 132475-93-5 2-isopropyl-5-nitroaniline 
• 170230-13-4 5-nitro-2-i-propylphenol 

Downstream Products

• 933045-61-5 2-i-propyl-5-(thiazol-2-ylamino)phenol 

Relevant articles and documents

COMPOUNDS AND METHODS FOR THE TREATMENT OF VIRUSES AND CANCER

The present invention relates to compounds according to the formula I: Where Ra is H or an optionally OH-substituted C1-C3 alkyl; R1 is OR1, an optionally substituted C4-12 carbocyclic group which may be saturated or unsaturated (including aromatic) or an optionally substituted heterocyclic group; R1 is an optionally substituted C1-C14 hydrocarbyl group or an optionally substituted heterocyclic group;; R2 , R3 and R4 are each independently H, an optionally substituted C1-C4 alkyl group (preferably CH3, CH2CH3 or CF3), halogen (preferably F, Cl, Br), OR, CN, NO2, a C1-C6 thioether, a C1-C6 thioester group, an optionally substituted CO2R group, an optionally substituted COR group or an optionally substituted OCOR group (preferably R4 is H); R is H or an optionally substituted C1-C6 alkyl group; RHET is an optionally substituted heterocyclic group; and pharmaceutically acceptable salts, solvates or polymorphs thereof.

Optimization of diarylamines as non-nucleoside inhibitors of HIV-1 reverse transcriptase

Following computational analyses, potential non-nucleoside inhibitors of HIV-1 reverse transcriptase have been pursued through synthesis and assaying for anti-viral activity. The general class Het-NH-Ph-U has been considered, where Het is an aromatic heterocycle and U is an unsaturated, hydrophobic group. Results for compounds with Het = 2-thiazoyl and 2-pyrimidinyl are the focus of this report.