85681-95-4

Basic information

• Product Name: 5-amino-2-propylphenol
• Synonyms: 5-amino-2-propylphenol;Einecs 288-233-6
• CAS NO: 85681-95-4
• Molecular Formula: C₉H₁₃NO
• Molecular Weight: 151.20562
• EINECS: 288-233-6
• Mol File: 85681-95-4.mol
• Article Data: 3

Chemical Properties

• Melting Point: 109-110 °C
• Boiling Point: 288°C at 760 mmHg
• Flash Point: 128°C
• Appearance: /
• Density: 1.084g/cm³
• Vapor Pressure: 0.00138mmHg at 25°C
• Refractive Index: 1.582
• PKA: 10.54±0.10(Predicted)
• CAS DataBase Reference: 5-amino-2-propylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 5-amino-2-propylphenol(85681-95-4)
• EPA Substance Registry System: 5-amino-2-propylphenol(85681-95-4)

Safety Data

• Hazardous Substances Data: 85681-95-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H13NO/c1-2-3-7-4-5-8(10)6-9(7)11/h4-6,11H,2-3,10H2,1H3

Upstream product

• 857621-80-8 2-acetoxy-4-acetylamino-1-propyl-benzene 
• 1821-39-2 2-propylaniline 
• 72635-75-7 5-nitro-2-propyl-aniline 
• 876314-60-2 5-nitro-2-n-propylphenol 
• 18979-60-7 4-propylresorcinol 
• 28583-72-4 N-(3-hydroxy-4-propylphenyl)acetamide 

Downstream Products

• 28583-72-4 N-(3-hydroxy-4-propylphenyl)acetamide 
• 857621-80-8 2-acetoxy-4-acetylamino-1-propyl-benzene 

Relevant articles and documents

SUBSTITUTED PYRIDOBENZODIAZEPINONE-DERIVATIVES AND USE THEREOF

The present application relates to novel (3-hydroxyphenyl)amino-substituted pyrido[2,3-b][1,5]benzodiazepin-5-one derivatives, to processes for preparation thereof, to the use thereof alone or in combination for treatment and/or prevention of diseases and to the use thereof for production of medicaments for treatment and/or prevention of diseases, especially of angiogenic disorders and hyperproliferative disorders in which neovascularization plays a role, for example ophthalmological disorders and cancers and tumours. Such treatments can be effected as monotherapy or else in combination with other medicaments or further therapeutic measures.

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.