14835-47-3

Usage

Uses

Used in Safety Glass Manufacturing:
1,2,4-Butanetriol, triacetate is used as a plasticizer for improving the flexibility and durability of safety glass. Its ability to enhance the properties of plastic materials makes it a valuable component in the production process.
Used in Chemical Industry:
1,2,4-Butanetriol, triacetate is used as a raw material in the synthesis of various chemical compounds. Its versatility in dissolving in common organic solvents allows for its use in a wide range of chemical reactions and processes.
Safety Precautions:
1,2,4-Butanetriol, triacetate is used with caution due to its potential to cause skin and eye irritation. It is essential to handle this chemical with care and store it in cool, dry places, away from heat sources and sunlight to prevent degradation.

Upstream product

• 50-00-0 formaldehyd 
• 591-87-7 Allyl acetate 
• 64-19-7 acetic acid 
• 107-18-6 allyl alcohol 
• 628-51-3 diacetoxymethane 
• 7664-93-9 sulfuric acid 
• 3068-00-6 D,L-1,2,4-butanetriol 
• 108-24-7 acetic anhydride 
• 7426-81-5 bis(allyloxy)methane 
• 2516-33-8 Cyclopropylmethanol 
• 546-67-8 lead(IV) tetraacetate 
• 38300-67-3 1,3,4-Tribromobutane 
• 127-08-2 potassium acetate 
• 627-27-0 homoalylic alcohol 

Relevant academic research and scientific papers

Oxidative Cyclization of Some γ- and δ-Hydroxy Olefins Induced by Tellurium Dioxide

TeO2 reacted with 2 equiv of a γ- or δ-hydroxy olefin in acetic acid containing LiCl.The resulting dialkyltellurium dichlorides are derivatives of furan, tetrahydrofuran, and 2,3-dihydrobenzofuran, formed via an internal cyclization.The dialkyltellurium dichlorides were reduced to their corresponding dialkyltellurides with use of Na2S2O5 or hydrazine hydrate.A mechanism is postulated involving an electrophilic attack by a solubilized tellurium species followed by an intramolecular nucleophilic attack by a hydroxy group.An analysis of the vicinal proton coupling constants indicated one preferred conformation of the dialkyltellurium dichlorides, where the oxygen atoms of the furan rings are coordinated to tellurium.

NaIO4/LiBr-mediated diastereoselective dihydroxylation of olefins: A catalytic approach to the prevost-woodward reaction

(Chemical Equation Presented) LiBr catalyzes efficiently the dihydroxylation of alkenes to afford syn and anti diols with excellent diastereoselectivity depending upon the use of NaIO4 (30 mol %) or PhI(OAc)2 (1 equiv), respectively, as the oxidants. The oxidation of non-benzylic halides has been achieved for the first time to afford the corresponding diols in excellent yields.