88795-87-3

Basic information

• Product Name: 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE
• Synonyms: 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE;1-(2,2-DIMETHYLTETRAHYDRO-2H-PYRAN-4-YL)-1-PENTANONE;1-(2,2-dimethyltetrahydro-2H-pyran-4-yl)-1-pentanone(SALTDATA: FREE)
• CAS NO: 88795-87-3
• Molecular Formula: C12H22O2
• Molecular Weight: 198.30188
• Mol File: 88795-87-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 270.7°C at 760 mmHg
• Flash Point: 100.1°C
• Appearance: /
• Density: 0.915g/cm³
• Vapor Pressure: 0.00674mmHg at 25°C
• Refractive Index: 1.439
• CAS DataBase Reference: 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE(88795-87-3)
• EPA Substance Registry System: 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE(88795-87-3)

Safety Data

• Hazardous Substances Data: 88795-87-3(Hazardous Substances Data)

Usage

Description

1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE is a chemical compound characterized by its molecular formula C12H22O. It is a ketone with a distinctive carbonyl group bonded to two carbon atoms, and is recognized for its fruity, floral scent.
Used in Fragrance Industry:
1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE is used as a fragrance additive for its appealing fruity and floral odor, enhancing the scent profiles of various perfumes and personal care products.
Used in Flavor Industry:
In the flavor industry, 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE is utilized as a flavoring agent, imparting its unique taste to food products, thereby enriching their sensory experience.
Used in Pharmaceutical Development:
1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE is also being explored for its potential pharmaceutical applications, particularly in the development of new drugs, capitalizing on its chemical properties for therapeutic benefits.
Safety Note:
As with many chemicals, 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-PENTAN-1-ONE should be handled with care and in accordance with established safety guidelines to ensure the well-being of users and the environment.

InChI:InChI=1/C12H22O2/c1-4-5-6-11(13)10-7-8-14-12(2,3)9-10/h10H,4-9H2,1-3H3

Upstream product

• 88795-74-8 ethyl ester of the 2-propyl-3-(2,2-dimethyltetryhydropyran-4-yl)-2,3-epoxypropionic acid 
• 34941-21-4 2,2-dimethyltetrahydro-2H-pyran-4-carbaldehyde 
• 109-65-9 1-bromo-butane 
• 60549-63-5 2,2-dimethyltetrahydro-2H-pyran-4-carbonitrile 

Relevant articles and documents

GENERAL RELATIONSHIPS IN THE OPENING OF THE OXIRANE RING DURING CLEAVAGE OF GLYCIDIC ACIDS

By investigation of the decarboxylation of 2,3-epoxy derivatives of acids with various structures it was shown that contrary to the existing theory about the essential opening of the β (C-O) bond in the oxirane ring there are many structural types of 2,3-epoxypropionic acids, in which opening of the α (C-O) bond in the oxirane ring occurs during decarboxylation.It was also shown that these two possible reaction paths can also arise during the decarboxylation of one 2,3-epoxypropionic acid.On the basis of the obtained data a general relationship is developed for theopening of the oxirane ring during the decarboxylation of 2,3-epoxypropionic acids with any structure, and this makes it possible to predict the structure of the obtained carbonyl compound.