55387-85-4

Usage

Uses

Used in Plastics Industry:
2-(2,2-DIETHOXYETHYL)-1,3-PROPANEDIOL is used as a plasticizer for enhancing the flexibility and durability of various polymers, such as PVC and other resins.
Used in Coatings Industry:
2-(2,2-DIETHOXYETHYL)-1,3-PROPANEDIOL is used as a solvent in coatings to improve their performance and application properties.
Used in Adhesives Industry:
2-(2,2-DIETHOXYETHYL)-1,3-PROPANEDIOL is used as a solvent in adhesives to enhance their bonding strength and durability.
Used in Other Industrial Applications:
2-(2,2-DIETHOXYETHYL)-1,3-PROPANEDIOL is also utilized as a solvent in various other industrial applications to improve product performance and processing efficiency.

InChI:InChI=1/C9H20O4/c1-3-12-9(13-4-2)5-8(6-10)7-11/h8-11H,3-7H2,1-2H3

Upstream product

• 21339-47-9 diethyl 2-(2,2-diethoxyethyl)malonate 
• 2032-35-1 Bromoacetaldehyde diethyl acetal 
• 105-53-3 diethyl malonate 

Downstream Products

• 144461-19-8 (R)-2-(2,2-diethoxyethyl)-1,3-propanediol monoacetate 
• 489441-63-6 ({4,4-diethoxy-2-[(phenylthio)methyl]butyl}thio)benzene 
• 489442-24-2 ethyl 4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-6-(phenylthio)-5-[(phenylthio)methyl]hexanoate 
• 489442-32-2 ethyl 4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-6-(phenylsulfonyl)-5-[(phenylsulfonyl)methyl]hexanoate 
• 489441-42-1 4-(phenylthio)-3-[(phenylthio)methyl]butanal 
• 489441-80-7 5-(phenylthio)-4-[(phenylthio)methyl]pentan-2-one 
• 489442-12-8 5-(phenylthio)-4-[(phenylthio)methyl]pentan-2-ol 
• 489442-18-4 (2E)-6-(phenylthio)-5-[(phenylthio)methyl]hex-2-en-1-ol 
• 489442-08-2 ethyl [(2E)-6-(phenylthio)methyl]hex-2-enoate 
• 489441-99-8 4-formyl-6-phenylsulfanyl-5-phenylsulfanylmethyl-hexanoic acid methyl ester 
• 489442-05-9 ethyl (2E)-2-methyl-6-(phenylthio)-5-[(phenylthio)methyl]hex-2-enoate 
• 489441-82-9 ethyl 3-isopropyl-6-(phenylthio)-5-[(phenylthio)methyl]hexanoate 
• 489441-84-1 ethyl 3-{3-(phenylthio)-2-[(phenylthio)methyl]propyl}pent-4-enoate 
• 489441-52-3 ethyl 3-isopropyl-6-(phenylsulfonyl)-5-[(phenylsulfonyl)methyl]hexanoate 

Relevant academic research and scientific papers

Regioselective alkylation of guanines using 2-acetoxytetrahydrofurans

Reaction of silylated guanine derivatives with 2-acetoxy-4-benzoyloxymethyltetrahydrofuran in DMF or NMP resulted in selective N-9 alkylation. This was used as the basis for a regioselective synthesis of the anti-viral agents famciclovir and penciclovir.

Synthesis of acyclic nucleoside derivatives

Methods and novel intermediates of the formula: wherein R6 and R7 are lower alkyl or benzyl or R6 and R7 taken together are —CH2CH2—, —CH2CH2CH2— or —CH2CH2CH2CH2CH2—, R8 is C1-C21 alkyl or a C2-C21 monounsaturated alkenyl, which may optionally be substituted with substitution substituents independently selected from the group consisting of hydroxy, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 alkoxy C1-C6 alkyl, C1-C6 alkanoyl, amino, halo, cyano, azido, oxo, mercapto and nitro, and R9 is an alcohol protecting group. The intermediates are useful for the preparation of acyclic nucleoside derivatives of the formula: where one of R1 and R2 is an amino acid acyl group and the other of R1 and R2 is a —C(O)C3-C21 saturated or monounsaturated, optionally substituted alkyl and R3 is OH or H; or a pharmaceutically acceptable salt thereof.

A VERSATILE SYNTHON APPROACH TO THE PREPARATION OF SOME PPHOSPHOLIPASE A2 INHIBITORS

A versatile route for the preparation of 2-ketomethylene phospholipids using dithiane chemistry is described.

New 4-substituted 2-alkoxytetrahydrofuran derivatives

The present invention describes a process to obtain 4-substituted 2--alkoxytetrahydrofuran derivatives of formula I. wherein,-R1 represents an alkyl or phenylalkyl radical; -R2 is hydrogen, C1-C4-acyl or C1

4-substituted-2-alkoxytetrahydrofuran derivatives

The present invention describes a process to obtain 4-substituted 2-alkoxytetrahydrofuran derivatives of formula I, STR1 wherein, --R1 represents an alkyl or phenylalkyl radical; --R2 is hydrogen, C1 -C4 -acryl