109066-05-9

Usage

Uses

Used in Pharmaceutical Production:
3-(MethoxyMethoxy)propanal is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the creation of a broad range of medicinal agents, contributing to the development of new treatments and therapies.
Used as a Flavoring Agent in Food and Beverages:
Leveraging its sweet and pungent aroma, 3-(MethoxyMethoxy)propanal is employed as a flavoring agent in the food and beverage industry. It enhances the taste and aroma profiles of various products, providing a pleasant sensory experience for consumers.
Used in Polymer Production:
3-(MethoxyMethoxy)propanal has potential applications in the production of polymers, where it can be used to create novel materials with specific properties. Its incorporation into polymer chemistry can lead to advancements in material science and the development of innovative products.
Used as a Solvent in Industrial Processes:
In various industrial applications, 3-(MethoxyMethoxy)propanal serves as a solvent, facilitating chemical reactions and processes. Its solvent properties make it a valuable component in a range of manufacturing and production activities.

Upstream product

• 52406-33-4 3-(methoxymethoxy)propanenitrile 
• 133884-35-2 3-methoxymethoxy-propan-1-ol 
• 17230-31-8 2-methoxy-1,3-dioxane 

Downstream Products

• 1027043-80-6 Toluene-4-sulfonic acid (2S,3S)-3-hydroxy-5-methoxymethoxy-2-((E)-styryl)-pentyl ester 
• 172225-75-1 (2S,3S)-5-Methoxymethoxy-2-((E)-styryl)-pentane-1,3-diol 
• 172225-76-2 (E)-(3S,4R)-1-Methoxymethoxy-4-methyl-6-phenyl-hex-5-en-3-ol 
• 809276-24-2 N-{(S)-3-[1-(2-Hydroxy-phenyl)-meth-(E)-ylideneaminooxy]-5-methoxymethoxy-pentanoyl}-benzamide 
• 809275-96-5 N-(3-hydroxy-5-methoxymethoxy-pentanoyl)-benzamide 
• 109066-06-0 3-benzyloxy-5-(methoxymethoxy)-1-pentene 
• 809275-90-9 (E)-N-(5-(methoxymethoxy)pent-2-enoyl)benzamide 
• 172225-74-0 (4R,5S)-3-[(2R,3S)-3-Hydroxy-5-methoxymethoxy-2-((E)-styryl)-pentanoyl]-4-methyl-5-phenyl-oxazolidin-2-one 

Relevant academic research and scientific papers

C-20 STEROID COMPOUNDS, COMPOSITIONS AND USES THEREOF TO TREAT TRAUMATIC BRAIN INJURY (TBI), INCLUDING CONCUSSIONS

The present invention relates to C-20 steroid compounds, compositions and methods of use thereof to treat, minimize and/or prevent traumatic brain injury (TBI), including severe TBI, moderate TBI and mild TBI, including concussions.

C-20 STEROID COMPOUNDS, COMPOSITIONS, AND USES THEREOF TO TREAT TRAUMATIC BRAIN INJURY (TBI), INCLUDING CONCUSSIONS

The present invention relates to C-20 steroid compounds, compositions and methods of use thereof to treat, minimize and/or prevent traumatic brain injury (TBI), including severe TBI, moderate TBI and mild TBI, including concussions.

SYNTHESIS OF ENT-PROGESTERONE AND INTERMEDIATES THEREOF

The present invention relates to the synthesis of ent-progesterone and intermediates thereof.

Using nucleophilic substitution reactions to understand how a remote alkyl or alkoxy substituent influences the conformation of eight-membered ring oxocarbenium ions

(Chemical Equation Presented) A remote alkoxy substituent strongly stabilizes one particular conformer of an eight-membered ring oxocarbenium ion by a through-space electrostatic effect. X-ray crystallographic analysis of a crystalline derivative proves t

Iridium-catalysed allylic substitution: Stereochemical aspects and isolation of IrIII complexes related to the catalytic cycle

Ir-catalysed allylic alkylations of enantiomerically enriched monosubstituted allylic acetates proceed with up to 87% retention of configuration using P(OPh)3 as ligand. High retention enantioselectivity of up to 86% ee in asymmetric allylic alkylations of achiral or racemic substrates is achieved with monodentate phosphorus amidites as ligands. Lithium N-tosylbenzylamide was identified as a suitable nucleophile for allylic aminations. Of particular importance is the use of lithium chloride as an additive, generally leading to increased enantioselectivities. Two (π-allyl)IrIII complexes were characterised by X-ray crystal structure analysis and spectroscopic data.

Stereoselectivity of Electrophile-Promoted Cyclizations of γ-Hydroxyalkenes. An Investigation of Carbohydrate-Derived and Model Substrates

We have investigated cyclization reactions of γ-hydroxyalkenes bearing an alkoxy or alkyl substituent on the allylic carbon.A variety of electrophiles N-bromosuccinimide, N-iodosuccinimide, iodine, mercury(II) acetate, mercury(II) trifluoroacetate, mercu