5309-43-3

Basic information

• Product Name: Pivalic acid (S)-2,3-dihydroxypropyl ester
• Synonyms: (-)-1-Pivalin;[S,(-)]-1-O-Pivaloyl-L-glycerol;2,2-Dimethylpropanoic acid (S)-2,3-dihydroxypropyl ester;Pivalic acid (S)-2,3-dihydroxypropyl ester;[R,(+)]-1-O-Pivaloyl-D-glycerol;2,2-Dimethylpropanoic acid (R)-2,3-dihydroxypropyl ester
• CAS NO: 5309-43-3
• Molecular Formula: C8H16O4
• Molecular Weight: 176.21
• Mol File: 5309-43-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Pivalic acid (S)-2,3-dihydroxypropyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Pivalic acid (S)-2,3-dihydroxypropyl ester(5309-43-3)
• EPA Substance Registry System: Pivalic acid (S)-2,3-dihydroxypropyl ester(5309-43-3)

Safety Data

• Hazardous Substances Data: 5309-43-3(Hazardous Substances Data)

Upstream product

• 3282-30-2 pivaloyl chloride 
• 100-79-8 (R,S)-2,2-dimethyl-1,3-dioxolane-4-methanol 
• 62244-21-7 (2,2-dimethyl-1,3-dioxolane-4-yl)methyl pivalate 
• 220499-01-4 2,2-dimethyl-propionic acid 2-chloro-1-chloromethyl-ethyl ester 
• 88837-78-9 isopropyl bis(4-methoxyphenyl)methyl ether 
• 256462-81-4 1-hydroxy-3-pivaloyloxypropan-2-one 

Relevant articles and documents

Copper(II) bromide as an efficient catalyst for acetal to bisarylmethyl ether interconversion

Transprotection of acetals to bis(methoxyphenyl)methyl (BMPM) ethers can be efficiently achieved in the presence of copper dibromide as catalyst in acetonitrile at room temperature. Acetals are conveniently and selectively converted to the corresponding m

Asymmetric synthesis of cyclic β-hydroxyallylsilanes via sequential allyltitanation-ring closing metathesis

Highly enantioenriched cyclic β-hydroxyallylsilanes have been prepared via enantioselective allylation of unsaturated aldehydes using a chiral allyltitanium reagent, followed by a ring-closing metathesis. Functionalized rings of various sizes have been sy