88795-86-2

Basic information

• Product Name: 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-BUTAN-1-ONE
• Synonyms: 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-BUTAN-1-ONE;1-(2,2-DIMETHYLTETRAHYDRO-2H-PYRAN-4-YL)-1-BUTANONE;1-(2,2-dimethyltetrahydro-2H-pyran-4-yl)-1-butanone(SALTDATA: FREE);1-(2,2-dimethyltetrahydro-2H-pyran-4-yl)butan-1-one
• CAS NO: 88795-86-2
• Molecular Formula: C11H20O2
• Molecular Weight: 184.2753
• Mol File: 88795-86-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 252.3°C at 760 mmHg
• Flash Point: 92.6°C
• Appearance: /
• Density: 0.92g/cm³
• Vapor Pressure: 0.0195mmHg at 25°C
• Refractive Index: 1.437
• CAS DataBase Reference: 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-BUTAN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-BUTAN-1-ONE(88795-86-2)
• EPA Substance Registry System: 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-BUTAN-1-ONE(88795-86-2)

Safety Data

• Hazardous Substances Data: 88795-86-2(Hazardous Substances Data)

Usage

Description

1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-BUTAN-1-ONE, a chemical compound with the molecular formula C11H20O2, is a cyclic ether derivative featuring a butanone group. It is recognized for its sweet, floral odor and is widely utilized in the fragrance and flavor industry for enhancing the scent of various products.

Uses

Used in Fragrance and Flavor Industry:
1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-BUTAN-1-ONE is used as a fragrance ingredient for its sweet, floral odor, making it suitable for adding a pleasant scent to perfumes, soaps, and cosmetics.
Used in Food Industry:
In the food industry, 1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-BUTAN-1-ONE is used as a flavoring agent to enhance the taste and aroma of various food products.
Used in Pharmaceutical Industry:
1-(2,2-DIMETHYL-TETRAHYDRO-PYRAN-4-YL)-BUTAN-1-ONE has potential applications in the pharmaceutical industry, where it serves as a precursor for the synthesis of various drugs, contributing to the development of new medicinal compounds.

InChI:InChI=1/C11H20O2/c1-4-5-10(12)9-6-7-13-11(2,3)8-9/h9H,4-8H2,1-3H3

Upstream product

• 874489-76-6 4-but-3-en-1-ynyl-2,2-dimethyl-3,6-dihydro-2H-pyran 
• 88795-73-7 ethyl ester of the 2-ethyl-3-(2,2-dimethyltetryhydropyran-4-yl)-2,3-epoxypropionic acid 
• 34941-21-4 2,2-dimethyltetrahydro-2H-pyran-4-carbaldehyde 
• 60549-63-5 2,2-dimethyltetrahydro-2H-pyran-4-carbonitrile 
• 106-94-5 propyl bromide 

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.