14202-14-3

Basic information

• Product Name: 3,5-DIMETHYLADAMANTANE-1-ACIDIC ACID
• Synonyms: 3,5-DIMETHYLADAMANTANE-1-ACIDIC ACID;3,5-DiMethyladaMantane-1-acetic acid;2-(3,5-DiMethyladaMantan-1-yl)acetic acid;3,5-DiMethyladaMantane-1-acetic acid;3,5-Dimethyladamantane-1-acetic acid 97%;2-(3,5-dimethyl-1-adamantyl)acetic acid;2-(3,5-dimethyl-1-adamantyl)ethanoic acid;3,5-Dimethyltricyclo[3.3.1.13,7]decane-1-acetic acid
• CAS NO: 14202-14-3
• Molecular Formula: C14H22O2
• Molecular Weight: 222.326
• Mol File: 14202-14-3.mol
• Article Data: 6

Chemical Properties

• Melting Point: 113-114℃ (ethanol water )
• Boiling Point: 339.2°C at 760 mmHg
• Flash Point: 166.8°C
• Appearance: White to off-white/Powder
• Density: 1.134±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 1.72E-05mmHg at 25°C
• Refractive Index: 1.548
• PKA: 4.72±0.10(Predicted)
• Water Solubility: Slightly soluble in water.
• CAS DataBase Reference: 3,5-DIMETHYLADAMANTANE-1-ACIDIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DIMETHYLADAMANTANE-1-ACIDIC ACID(14202-14-3)
• EPA Substance Registry System: 3,5-DIMETHYLADAMANTANE-1-ACIDIC ACID(14202-14-3)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 14202-14-3(Hazardous Substances Data)

Usage

Uses

A commonly used as an organic reagent and pharmaceutical intermediate.

InChI:InChI=1/C14H22O2/c1-12-3-10-4-13(2,7-12)9-14(5-10,8-12)6-11(15)16/h10H,3-9H2,1-2H3,(H,15,16)

Upstream product

• 707-37-9 1,3-dimethyl-5-adamantanol 
• 941-37-7 3,5-dimethyl-1-bromoadamantane 
• 41281-65-6 3.5-Dimethyladamantanylmalonsaeure 
• 75-35-4 1,1-Dichloroethylene 
• 101821-77-6 3,5-dimethyladamantan-1-yl nitrate 
• 702-79-4 1,3-dimethyladamantane 
• 74-86-2 acetylene 

Downstream Products

• 50847-70-6 2-(3,5-Dimethyl-1-adamantyl)-ethanol-1 

Relevant articles and documents

Bicycloheteroaryl compounds as P2X7 modulators and uses thereof

Bicycloheteroaryl compounds are disclosed that have a formula represented by the following: The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including huma

NOUVEAUX DECONTAMINANTS. DESTRUCTION DE TOXIQUES ORGANOPHOSPHORES OU SOUFRES PAR DES PERACIDES MONO-, BI- ET TRICYCLIQUES SATURES

New peroxycarboxylic and peroxyacetic acids have been tested for the destruction of some organophosphorus compounds and mustards.The peroxyacids used have monocyclic, bicyclic or tricyclic structures.These are very reactive against paraoxon or HD and the addition of certain surfactants enhances the reaction rate.Very short half-live times are obtained with these compounds.

ADAMANTANOL NITRATES IN NUCLEOPHILIC SUBSTITUTION REACTIONS

-