24556-16-9

Basic information

• Product Name: Isopropyl 1-adamantanecarboxylate
• Synonyms: 1-Adamantanecarboxylic acid isopropyl ester;Isopropyl 1-adamantanecarboxylate
• CAS NO: 24556-16-9
• Molecular Formula: C₁₄H₂₂O₂
• Molecular Weight: 222.32328
• Mol File: 24556-16-9.mol
• Article Data: 5

Chemical Properties

• Melting Point: 29-30℃
• Boiling Point: 265.9±8.0℃ (760 Torr)
• Flash Point: 115.0±6.0℃
• Appearance: /
• Density: 1.083±0.06 g/cm3 (20 ºC 760 Torr)
• CAS DataBase Reference: Isopropyl 1-adamantanecarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Isopropyl 1-adamantanecarboxylate(24556-16-9)
• EPA Substance Registry System: Isopropyl 1-adamantanecarboxylate(24556-16-9)

Safety Data

• Hazardous Substances Data: 24556-16-9(Hazardous Substances Data)

Usage

General Description

Isopropyl 1-adamantanecarboxylate, also known as IPAC, is a chemical compound that belongs to the class of adamantane carboxylates. It is a colorless, odorless liquid with a relatively low boiling point and is often used as a solvent or a chemical intermediate in various industries. IPAC is known for its high solvency and low toxicity, making it a popular choice for cleaning and degreasing applications. It is also used as a flavoring agent in the food and beverage industry, and as a fragrance ingredient in the perfume and cosmetic industry. Additionally, IPAC has been studied for its potential pharmacological properties, such as its anti-inflammatory and antiviral effects.

InChI:InChI=1S/C14H22O2/c1-9(2)16-13(15)14-6-10-3-11(7-14)5-12(4-10)8-14/h9-12H,3-8H2,1-2H3

Upstream product

• 2094-72-6 1-Adamantanecarbonyl chloride 
• 828-51-3 1-Adamantanecarboxylic acid 
• 75-30-9 2-iodo-propane 

Downstream Products

• 23074-42-2 1-adamantanecarbonitrile 

Relevant articles and documents

Reduction of Carboxylic Acid with 2-Propanol over Hydrous Zirconium Oxide

The vapor-phase reduction of carboxylic acids with 2-propanol was found to proceed efficiently over hydrous zirconium(IV) oxide, and the corresponding alcohols were obtained in high yield.Esters were also reduced.

Synthesis and Properties of a Series of Sterically Hindered Guanidine Bases

By the reaction of Vilsmeier salts, derived from tetra-alkylureas or from tetra-alkylthioureas, with primary aliphatic amines, a series of sterically hindered penta-alkyl guanidines has been prepared. 2-t-Butyl-1',1',3'',3''-tetramethylguanidine and pentaisopropylguanidine combine ease of preparation with a range of resistance to alkylating agents.Preliminary experiments indicate that these inexpensive bases will useful in organic synthesis.

The Synthesis and Properties of a Series of Strong but Hindered Organic Bases

A series of highly hindered N1,N2,N2,N3,N3-penta-alkylguanidines has been synthesised from inexpensive starting materials; these strong bases show interesting effects in organic synthesis.