100181-71-3

Basic information

• Product Name: isobutyl 3,4-epoxybutyrate
• Synonyms: ISOBUTYL 3,4-EPOXYBUTYRATE
• CAS NO: 100181-71-3
• Molecular Formula: C8H14O3
• Molecular Weight: 158.19
• EINECS: 401-920-9
• Mol File: 100181-71-3.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 194.8°C at 760 mmHg
• Flash Point: 85.6°C
• Appearance: /
• Density: 1.042g/cm³
• Vapor Pressure: 0.433mmHg at 25°C
• Refractive Index: 1.445
• Water Solubility: 5300 mg l-1 (e)
• CAS DataBase Reference: isobutyl 3,4-epoxybutyrate(CAS DataBase Reference)
• NIST Chemistry Reference: isobutyl 3,4-epoxybutyrate(100181-71-3)
• EPA Substance Registry System: isobutyl 3,4-epoxybutyrate(100181-71-3)

Safety Data

• Hazardous Substances Data: 100181-71-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H14O3/c1-6(2)4-11-8(9)3-7-5-10-7/h6-7H,3-5H2,1-2H3

Upstream product

• 135681-62-8 isobutyl (3RS)-3-hydroxy-4-methanesulfonyloxybutyrate 
• 108-05-4 vinyl acetate 
• 10213-10-2 sodium tungstate (VI) dihydrate 
• 75-34-3 1,1-dichloroethane 
• 10108-86-8 octyltrimethylammonium chloride 
• 24342-03-8 isobutyl vinylacetate 

Downstream Products

• 68108-18-9 (4S)-4-hydroxypyrrolidin-2-one 

Relevant articles and documents

A Very Efficient Alkene Epoxidation by Magnesium Monoperoxyphthalate Catalysed by Manganese Porphyrins

Mn-porphyrins catalyse the epoxidation of various alkenes by magnesium monoperoxyphthalate: with 0.125-1 percent of tetra-2,6-dichlorophenylporphirinatomanganese(III) acetate as a catalyst, alkene conversion is nearly complete within 0.5-5 minutes at 0 de

Method for the preparation of alkyl esters of 3,4-epoxybutyric acid

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Enzymatic Hydrolysis of Alkyl 3,4-Epoxybutyrates. A New Route to (R)-(-)-Carnitine Chloride

The enzyme-catalyzed hydrolysis of alkyl 3,4-epoxybutyrates to the corresponding epoxy acids is reported.By using esterases the reaction occurred with good stereoselectivity leading to optically active unreacted esters of R configuration.With proteases the stereoselectivity was reversed, and the S enantiomer of the unreacted ester was recovered, albeit in lover enantiomeric excess.Finally, upon preliminary optimization of the reaction conditions, a new synthesis of (R)-(-)-carnitine chloride by the successive use of a stereoselective and of a nonstereoselective enzymatic hydrolysis is shown.