84223-13-2

Basic information

• Product Name: 2-Propanone, 1-butoxy- (9CI)
• Synonyms: 2-Propanone, 1-butoxy- (9CI)
• CAS NO: 84223-13-2
• Molecular Formula: C₇H₁₄O₂
• Molecular Weight: 130.18486
• Product Categories: ACETYLGROUP
• Mol File: 84223-13-2.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Propanone, 1-butoxy- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propanone, 1-butoxy- (9CI)(84223-13-2)
• EPA Substance Registry System: 2-Propanone, 1-butoxy- (9CI)(84223-13-2)

Safety Data

• Hazardous Substances Data: 84223-13-2(Hazardous Substances Data)

Upstream product

• 89530-91-6 butoxyacetonitrile 
• 2426-08-6 glycidyl n-butyl ether 
• 201230-82-2 carbon monoxide 
• 5131-66-8 1-butoxy-2-propanol 
• 929-27-1 3-butoxy-1-propyne 
• 79629-36-0 1-(2,3-dibromo-propoxy)-butane 
• 98451-40-2 3-n-butoxy-1,2-propanediol 

Downstream Products

• 51-66-1 4-methoxyacetanilide 
• 103-84-4 Acetanilid 
• 21801-24-1 1-(4-cinnamylpiperazin-1-yl)ethan-1-one 
• 16078-30-1 1-Acetyl-2,3-dihydro-1H-indole 

Relevant articles and documents

EMULSIFIABLE CONCENTRATES

Embodiments of the present invention relate to compositions that can be used as emulsifiable concentrates in the agriculture industry. In one aspect, a composition comprises (a) 5 weight percent or more of a compound soluble in at least one of Ν,Ν-dialkyl fatty amide, an aromatic ketone, an alkyl ketone, a cyclic ketone, or an aromatic hydrocarbon solvent; and (b) an ether ketone solvent according to Formula 1, as described herein, wherein R1 is a linear or branched alkyl group having 4 to 8 carbon atoms, wherein R2 is CH3 or CH2CH3, wherein x is 0, 1, or 2, wherein R3 is CH3 when R2 is CH3, and wherein R3 is CH2CH3 when R2 is CH2CH3.

Practical β-lactone synthesis: Epoxide carbonylation at 1 atm

A readily prepared bimetallic catalyst is capable of effecting epoxide carbonylation to produce β-lactones at substantially lower CO pressures than previously reported catalyst systems. A functionally diverse array of β-lactones is produced in excellent yields at CO pressures as low as 1 atm. This procedure allows for epoxide carbonylation on a multigram scale without the requirement of specialized, high-pressure equipment.

2-chloro-1,3-dimethylimidazolinium chloride. 3. Utility for chlorination, oxidation, reduction, and rearrangement reactions

2-Chloro-1,3-dimethylimidazolinium chloride (1), which can act as a powerful dehydrating equivalent to DCC (2), is also applicable to chlorination, oxidation, reduction, and rearrangement under nearly neutral conditions. The utility of 1 for these reactions is described.