27684-79-3

Basic information

• Product Name: desacetylpractolol
• Synonyms: desacetylpractolol;2-Propanol, 1-(4-aminophenoxy)-3-[(1-methylethyl)amino]-
• CAS NO: 27684-79-3
• Molecular Formula: C₁₂H₂₀N₂O₂
• Molecular Weight: 224.2994
• Mol File: 27684-79-3.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 407.2°Cat760mmHg
• Flash Point: 200°C
• Appearance: /
• Density: 1.092g/cm³
• Vapor Pressure: 2.32E-07mmHg at 25°C
• Refractive Index: 1.549
• CAS DataBase Reference: desacetylpractolol(CAS DataBase Reference)
• NIST Chemistry Reference: desacetylpractolol(27684-79-3)
• EPA Substance Registry System: desacetylpractolol(27684-79-3)

Safety Data

• Hazardous Substances Data: 27684-79-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H20N2O2/c1-9(2)14-7-11(15)8-16-12-5-3-10(13)4-6-12/h3-6,9,11,14-15H,7-8,13H2,1-2H3

Upstream product

• 125228-75-3 4-nitrophenyl 2-oxiranylmethyl ether 
• 100-02-7 4-nitro-phenol 
• 6673-35-4 practolol 

Downstream Products

• 111218-78-1 2-Chloro-4-<4-(3'-isopropylamino-2'-oxypropoxy)phenylamino>-6,7-dimethoxyquinazoline 
• 6673-33-2 1-(4-Ethoxycarbonylaminophenoxy)-2-hydroxy-3-isopropylaminopropan 
• 72224-51-2 N-[4-(2-hydroxy-3-isopropylamino-propoxy)-phenyl]-3-(4-phenyl-piperazin-1-yl)-propionamide 
• 265669-12-3 3-[4-(3-iodoprop-2-enyloxycarbonylamino)phenoxy]-1-N-(tert-butoxycarbonyl)isopropylaminopropan-2-ol 
• 265669-10-1 3-[4-(prop-2-ynyloxycarbonylamino)phenoxy]-1-(N-tert-butoxycarbonyl)isopropylaminopropan-2-ol 
• 175532-42-0 3-[4-(amino)phenoxy]-11-N-(tertbutoxycarbonyl)isopropylaminopropan-2-ol 
• 65854-89-9 1-(p-iodophenoxy)-3-isopropylamino-2-propanol 
• 280580-27-0 4-Anilino-5-chloro-2-{4-[2-hydroxy-3-(isopropylamino)propoxy]anilino}pyrimidine 

Relevant articles and documents

2,4-DIAMINO PYRIMIDINE COMPOUNDS HAVING ANTI-CELL PROLIFERATIVE ACTIVITY

A pyrimidine derivative of formula (I) wherein, for example, R1 is hydrogen, (1-6C)alkyl, (3-5C)alkenyl or (3-5C)alkynyl; Q1 and Q2 are independently selected from phenyl, naphthyl, indanyl and 1,2,3,4-tetrahydronaphthyl; and one or both of Q1 and Q2 bear

The Synthesis and Potassium Channel Blocking Activity of Some (4-Methanesulfonamidophenoxy)propanolamines as Potential Class III Antiarrhythmic Agents

The synthesis of 22 (4-methanesulfonamidophenoxy)propanolamines and their testing on isolated guinea pig cardiac myocytes, on isolated preparations from guinea pig atria, and on rat blood pressure are described.Secondary amines in the series (11a-f) showe

On the synthesis of compounds with β-adrenergic activity

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