52464-51-4

Basic information

• Product Name: 2-(pentyloxy)aniline
• Synonyms: 2-(Pentyloxy)aniline; benzenamine, 2-(pentyloxy)-
• CAS NO: 52464-51-4
• Molecular Formula: C₁₁H₁₇NO
• Molecular Weight: 179.2588
• Mol File: 52464-51-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 283.5°C at 760 mmHg
• Flash Point: 121.9°C
• Density: 0.986g/cm³
• Vapor Pressure: 0.00316mmHg at 25°C
• Refractive Index: 1.525
• CAS DataBase Reference: 2-(pentyloxy)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(pentyloxy)aniline(52464-51-4)
• EPA Substance Registry System: 2-(pentyloxy)aniline(52464-51-4)

Safety Data

• Hazardous Substances Data: 52464-51-4(Hazardous Substances Data)

Usage

General Description

2-(pentyloxy)aniline is a chemical compound with the molecular formula C12H17NO. It is an aniline derivative with a pentyl group attached to the oxygen atom. 2-(pentyloxy)aniline is commonly used as an intermediate in the synthesis of various organic compounds and pharmaceuticals. It has potential applications in the production of dyes, pigments, and polymers. Additionally, 2-(pentyloxy)aniline may also be used in research and development in the fields of organic chemistry and medicinal chemistry. It is important to handle this chemical with care and follow proper safety precautions due to its potential health hazards.

Upstream product

• 110-53-2 1-Bromopentane 
• 1624-53-9 2-(benzylideneamino)phenol 
• 614-80-2 2-(acetylamino)phenol 
• 95-55-6 2-amino-phenol 
• 55792-54-6 acetic acid-(2-pentyloxy-anilide) 
• 86255-27-8 silver(I) 2-nitrophenoxide 
• 628-17-1 amyl iodide 
• 65347-86-6 (2-Pentyloxy-phenyl)-carbamic acid 2-morpholin-4-yl-ethyl ester 
• 39645-91-5 1-nitro-2-(pentyloxy)benzene 
• 88-75-5 2-hydroxynitrobenzene 

Downstream Products

• 859934-94-4 (2-iodo-phenyl)-pentyl ether 
• 32223-65-7 2-n-Pentyloxyphenylisocyanat 
• 98772-15-7 6-Oxo-2-(2-pentyloxy-phenylamino)-1,6-dihydro-pyrimidine-5-carboxylic acid 
• 98771-63-2 6-Oxo-2-(2-pentyloxy-phenylamino)-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester 

Relevant articles and documents

Determination of critical micellar concentration of homologous 2-alkoxyphenylcarbamoyloxyethyl-morpholinium chlorides

The critical micellar concentrations of selected alkyloxy homologues of local anesthetic 4-(2-[(2-alkoxyphenyl)carbamoyl]oxy ethyl)morpholin-4-ium chloride with nc = 2, 4, 5, 6, 7, 8, and 9 carbons in alkyloxy tail were determined by absorption spectroscopy in the UV–vis spectral region with the use of a pyrene probe. Within the homologous series of the studied amphiphilic compounds, the ln(cmc) was observed to be dependent linearly on the number of carbon atoms nc in the hydrophobic tail: ln(cmc) = 0.705–0.966 nc. The Gibbs free energy, necessary for the transfer of the methylene group of the alkoxy chain from the water phase into the inner part of the micelle at the temperature of 25?C and pH ≈ 4.5–5.0, was found to be ?2.39 kJ/mol. The experimentally determined cmc values showed good correlations with the predicted values of the bulkiness of the alkoxy tail expressed as the molar volume of substituent R, as well as with the surface tension of the compounds.

Investigations on the 4-quinolone-3-carboxylic acid motif. 4. Identification of new potent and selective ligands for the cannabinoid type 2 receptor with diverse substitution patterns and antihyperalgesic effects in mice

Experimental evidence suggests that selective CB2 receptor modulators may provide access to antihyperalgesic agents devoid of psychotropic effects. Taking advantage of previous findings on structure-activity/selectivity relationships for a class of 4-quin

The kinetics of alkaline hydrolysis of morpholinoethylesters of 2-alkyloxyphenylcarbamic acid

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