88795-91-9

Basic information

• Product Name: 1-(4-ISOPROPOXY-PHENYL)-HEXAN-2-ONE
• Synonyms: 1-(4-ISOPROPOXY-PHENYL)-HEXAN-2-ONE
• CAS NO: 88795-91-9
• Molecular Formula: C₁₅H₂₂O₂
• Molecular Weight: 234.33398
• Mol File: 88795-91-9.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(4-ISOPROPOXY-PHENYL)-HEXAN-2-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-ISOPROPOXY-PHENYL)-HEXAN-2-ONE(88795-91-9)
• EPA Substance Registry System: 1-(4-ISOPROPOXY-PHENYL)-HEXAN-2-ONE(88795-91-9)

Safety Data

• Hazardous Substances Data: 88795-91-9(Hazardous Substances Data)

Usage

Chemical family

Ketones

Usage

Research chemical

Psychoactive properties

Stimulant

Recreational use

Often associated with recreational drug use

Physical appearance

White crystalline powder

Administration methods

Ingestion, inhalation, or injection

Effects

Increased energy, heightened senses, and euphoria

Regulation

Use and distribution are often regulated due to potential for misuse and dependency

Upstream product

• 18962-05-5 4-isopropoxybenzaldehyde 
• 88795-81-7 ethyl ester of the 2-butyl-3-(p-isopropoxyphenyl)-2,3-epoxypropionic acid 
• 85153-52-2 ethyl ester of the 2-chlorocapronic acid 
• 615-96-3 Ethyl 2-bromohexanoate 
• 344872-08-8 2-butyl-3-(p-isopropoxyphenyl)-2,3-epoxypropionic acid 

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.