Chinese  Japanese  Germany

Nafenopin

CAS No.3771-19-5
Chemical Name:Nafenopin
Synonyms:TPIA;Melipan;Su-13437;Nafenopin;C-13437Su;CIBA-13437Su;2-methyl-2-(4-tetralin-1-ylphenoxy)propionic acid;2-METHYL-2-PARA-(1,2,3,4-TETRAHYDRO-1-NAPHTHYL)PHENOXYPROPIONICACID;2-methyl-2-[4-(1,2,3,4-tetrahydronaphthalen-1-yl)phenoxy]propanoic acid
CBNumber:CB61116627
Molecular Formula:C20H22O3
Formula Weight:310.391
MOL File:3771-19-5.mol
Nafenopin Property
Safety

Nafenopin Chemical Properties,Usage,Production

General Description
Crystals.
Reactivity Profile
An organic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in Nafenopin to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible.
Fire Hazard
Flash point data for Nafenopin are not available. Nafenopin is probably combustible.
Nafenopin Preparation Products And Raw materials
Raw materials
Preparation Products
Nafenopin Suppliers      Global( 7)Suppliers     
SupplierTelFaxEmailCountryProdListAdvantage
Shanghai AQBioPharma Co., Ltd. +86 (21) 51370935/8002 13661411401+86 (21) 51370935/8011 QQ:1142668814sales@aqbiopharma.com.cnCHINA 1267 58
 
3771-19-5(Nafenopin)Related Search:
2-methyl-2-(4-methylphenoxy)propanoic acid AKOS B013930 Nafenopin 2-(4-ISOPROPYLPHENOXY)PROPANOIC ACID 2-(4-ETHYLPHENOXY)PROPANOIC ACID 2-(4-ISOPROPYLPHENOXY)-2-METHYLPROPANOIC ACID
3771-19-5 Nafenopin C20H22O3 2-METHYL-2-PARA-(1,2,3,4-TETRAHYDRO-1-NAPHTHYL)PHENOXYPROPIONICACID C-13437Su CIBA-13437Su Melipan Su-13437 TPIA 2-methyl-2-(4-tetralin-1-ylphenoxy)propionic acid 2-methyl-2-[4-(1,2,3,4-tetrahydronaphthalen-1-yl)phenoxy]propanoic acid
Copyright 2016 © ChemicalBook. All rights reserved