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Isopropyl 1-adamantanecarboxylate, also known as IPAC, is a colorless, odorless liquid chemical compound belonging to the class of adamantane carboxylates. It is characterized by a relatively low boiling point, high solvency, and low toxicity, making it suitable for a variety of applications across different industries.

24556-16-9

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24556-16-9 Usage

Uses

Used in Cleaning and Degreasing Applications:
Isopropyl 1-adamantanecarboxylate is used as a solvent for its high solvency and low toxicity, making it effective in cleaning and degreasing processes, particularly in industrial settings where efficient removal of contaminants and residues is required.
Used in the Food and Beverage Industry:
Isopropyl 1-adamantanecarboxylate is used as a flavoring agent due to its ability to impart specific tastes and aromas to food and beverages, enhancing the overall sensory experience for consumers.
Used in the Perfume and Cosmetic Industry:
Isopropyl 1-adamantanecarboxylate is used as a fragrance ingredient in perfumes and cosmetics, leveraging its aromatic properties to create appealing scents for personal care products.
Used in Pharmaceutical Research:
Isopropyl 1-adamantanecarboxylate is studied for its potential pharmacological properties, such as anti-inflammatory and antiviral effects, indicating its possible use in the development of new drugs and therapies.
Used in Chemical Intermediates:
Isopropyl 1-adamantanecarboxylate serves as a chemical intermediate in the synthesis of various compounds, contributing to the production of a wide range of chemical products and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 24556-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,5 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24556-16:
(7*2)+(6*4)+(5*5)+(4*5)+(3*6)+(2*1)+(1*6)=109
109 % 10 = 9
So 24556-16-9 is a valid CAS Registry Number.
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

24556-16-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name propan-2-yl adamantane-1-carboxylate

1.2 Other means of identification

Product number -
Other names isopropyl adamantane-1-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24556-16-9 SDS

24556-16-9Downstream Products

24556-16-9Relevant academic research and scientific papers

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

Takahashi, Kyoko,Shibagaki, Makoto,Kuno, Hideyuki,Matsushita, Hajime

, p. 1141 - 1144 (2007/10/02)

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

Barton, Derek H. R.,Elliott, John D.,Gero, Stephan D.

, p. 2085 - 2090 (2007/10/02)

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.

Synthesis of 1-adamantyl and 1-adamantylmethyl alkyl ketones

Grava, I. Ya.,Polis, Ya. Yu.,Lidak, M. Yu.,Liepin'sh, E. E.,Shatts, V. D.,et al.

, p. 679 - 686 (2007/10/02)

The reaction of 1-adamantanecarboxylic and 1-adamantylacetic acids with Grignard reagents in the presence of cuprous chloride or iodide gave the corresponding ketones.

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

Barton, Derek H. R.,Elliott, John D.,Gero, Stephen D.

, p. 1136 - 1137 (2007/10/02)

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.

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