64952-14-3

Basic information

• Product Name: (2R)-3-hydroxy-2-[(1R)-1-methoxy-2-oxoethoxy]propanal
• CAS NO: 64952-14-3
• Molecular Formula: C₆H₁₀O₅
• Molecular Weight: 162.1406
• Mol File: 64952-14-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 231.3°C at 760 mmHg
• Flash Point: 90.7°C
• Density: 1.217g/cm³
• Vapor Pressure: 0.0119mmHg at 25°C
• Refractive Index: 1.44
• CAS DataBase Reference: (2R)-3-hydroxy-2-[(1R)-1-methoxy-2-oxoethoxy]propanal(CAS DataBase Reference)
• NIST Chemistry Reference: (2R)-3-hydroxy-2-[(1R)-1-methoxy-2-oxoethoxy]propanal(64952-14-3)
• EPA Substance Registry System: (2R)-3-hydroxy-2-[(1R)-1-methoxy-2-oxoethoxy]propanal(64952-14-3)

Safety Data

• Hazardous Substances Data: 64952-14-3(Hazardous Substances Data)

Usage

Description

(2R)-3-hydroxy-2-[(1R)-1-methoxy-2-oxoethoxy]propanal is a chiral chemical compound characterized by a propanal backbone with a hydroxy and a methoxy group, as well as an oxoethoxy group. Its (2R) configuration denotes a specific three-dimensional arrangement of atoms, which may influence its properties and reactivity.

Uses

Used in Pharmaceutical Industry:
(2R)-3-hydroxy-2-[(1R)-1-methoxy-2-oxoethoxy]propanal is used as a potential candidate for pharmaceutical applications due to its unique molecular structure and chiral configuration. Its properties and reactivity may be of interest for the development of new drugs or drug delivery systems.
Used in Chemical Industry:
In the chemical industry, (2R)-3-hydroxy-2-[(1R)-1-methoxy-2-oxoethoxy]propanal may be utilized as an intermediate or a building block in the synthesis of various complex organic compounds. Its specific configuration and functional groups could be advantageous for creating novel chemical entities with tailored properties.

Upstream product

• 22277-65-2 Methyl mannoside 
• 709-50-2 methyl beta-D-glucopyranoside 
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Downstream Products

• 132817-56-2 7-O-<2,3,6-Trideoxy-3-<6(S)-hydroxymethyl-2(R)-methoxymorpholin-4-yl>-α-L-lyxo-hexopyranosyl>-ε-rhodomycinone 
• 127903-57-5 7-O-<2,3,6-Trideoxy-3-<6(S)-hydroxymethyl-2(R)-methoxymorpholin-4-yl>-α-L-lyxo-hexopyranosyl>-ε-isorhodomycinone 
• 4631-21-4 methyl 3-nitro-β-D-3-deoxy-glucopyranoside 
• 72523-27-4 (2R,4aR,6R,7R,8R,8aS)-6-Methoxy-8-nitro-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 
• 206126-54-7 Acetic acid (2R,4aR,6R,7R,8S,8aS)-6-methoxy-8-nitro-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 131652-54-5 methyl 4,6-O-benzylidene-3-C-carbamoyl-3-C-cyano-3-deoxy-β-D-glucopyranoside 
• 131652-55-6 Acetic acid (4aR,6R,7R,8S,8aS)-8-carbamoyl-8-cyano-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 10563-74-3 2-[(R)-1-methoxy-2-(4-nitro-benzoyloxy)-ethoxy]-1,3-bis-(4-nitro-benzoyloxy)-propane 
• 14218-26-9 3-Nitro-3-deoxy-β-D-mannopyranose-methylglucosid 
• 14218-25-8 3-Nitro-3-deoxy-β-D-galactopyranose-methylglucosid 

Relevant articles and documents

Synthesis of 3-oxagranatane-type alkaloid analogs from carbohydrates

3-Oxagranatane derivatives have been synthesized from dialdehydes obtained by the periodate oxidation of D-glucopyranosides. Reduction of the carbonyl group and removal of the substituents afforded bicyclic iminosugar analogs.

Carbohydrate-Based Small-Molecule Scaffolds for the Construction of Universal Pharmacophore Mapping Libraries

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