40166-30-1

Usage

Uses

Used in Chemical Synthesis:
3-BENZYLOXY-2,2-DIMETHOXY-PROPAN-1-OL is used as a versatile intermediate in chemical synthesis for the production of various organic compounds. Its ability to react with other chemicals allows for the creation of a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-BENZYLOXY-2,2-DIMETHOXY-PROPAN-1-OL is used as a building block for the synthesis of various pharmaceuticals. Its reactivity with other chemicals makes it an essential component in developing new medications.
Used as a Solvent:
3-BENZYLOXY-2,2-DIMETHOXY-PROPAN-1-OL is also used as a solvent in various applications due to its ability to dissolve a wide range of substances. This makes it a valuable asset in industries that require solvents for processes such as cleaning, manufacturing, and more.
It is important to handle 3-BENZYLOXY-2,2-DIMETHOXY-PROPAN-1-OL with care, as it can be hazardous if not properly managed.

InChI:InChI=1/C12H18O4/c1-14-12(9-13,15-2)10-16-8-11-6-4-3-5-7-11/h3-7,13H,8-10H2,1-2H3

Upstream product

• 100-44-7 benzyl chloride 
• 153214-82-5 2,2-dimethoxypropane-1,3-diol 
• 100-39-0 benzyl bromide 

Downstream Products

• 17325-85-8 (2S)-3-(benzyloxy)propane-1,2-diol 
• 56552-80-8 (R)-3-benzyloxy-1,2-propanediol 
• 121787-44-8 (-)-1-O-acetyl-3-O-benzylpropane-1,2,3-triol 
• 87385-73-7 1-benzyloxy-3-acetoxypropan-2-one 
• 151212-86-1 (+)-1-O-acetyl-3-O-benzylpropane-1,2,3-triol 
• 17325-86-9 (+)-(S)-1,2-di-O-acetyl-3-O-benzylpropane-1,2,3-triol 
• 153214-79-0 1-(benzyloxy)-3-hydroxypropan-2-one 

Relevant academic research and scientific papers

Synthesis and antimicrobial evaluation of oxazole-2(3H)-thione and 2-alkylsulfanyl-1,3-oxazole derivatives

The preparation of oxazole-2(3H)-thiones (OXTs) by condensation of thiocyanic acid on α-hydroxycarbonyl substrates has been revisited. Extension to more complex scaffolds afforded chiral OXTs, whereas carbohydrate-fused 2-alkylsulfanyl-1,3-oxazolines led

Aromatic or chiral heterocycle - Balance between 1,3-oxazoline-2-thione and 1,3-oxazolidine-2-thione

1,3-Oxazoline-2-thiones (OXT) and bis-1,3-oxazol-idine-2-thiones (bis-OZT) were selectively prepared depending on the conditions and starting materials used, and then underwent some N- and S-selective reactions. Georg Thieme Verlag Stuttgart.

Baker's yeast mediated reduction of dihydroxyacetone derivatives

Several monoprotected dihydroxyacetone derivatives 4a-d and their acetates 5a-d were prepared and subjected to biotransformation with baker's yeast. The simple chemical modification of the substrates (i.e. transforming the relatively small hydrophilic hyd

Synthesis and Ruthenium-Catalyzed Enantioselective Hydrogenation of 3-O-Substituted 1,3-dihydroxypropan-2-ones

A number of 3-O-substituted 1,3-dihydroxypropan-2-ones have been synthesized in view of their potential use as prochiral precursors of optically active glycerols.Indeed, the oxo-ethers have been reduced to the corresponding 3-O-substituted glycerols via c