(R)-Methyl 2,3-dihydroxypropanoate

95%

Reagent Code: #37409
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CAS Number 18289-89-9

science Other reagents with same CAS 18289-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 120.10392 g/mol
Formula C₄H₈O₄
badge Registry Numbers
MDL Number MFCD06204263
thermostat Physical Properties
Boiling Point 140 ℃(Press: 15 Torr)
inventory_2 Storage & Handling
Density 1.2795 g/cm3
Storage 2-8℃

description Product Description

(R)-Methyl 2,3-dihydroxypropanoate is a chiral building block primarily utilized in the synthesis of pharmaceutical intermediates, particularly for antiviral nucleoside analogs and other enantiomerically pure compounds. Its (R)-configuration and dihydroxy functionality enable asymmetric synthesis routes to biologically active molecules, such as those used in carbohydrate chemistry and drug development for infectious diseases. It also serves as a precursor in fine chemicals and agrochemicals, where stereospecificity is critical for efficacy. In organic synthesis, it is employed to construct complex structures with high purity, contributing to advanced materials and specialty applications.

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Test Parameter Specification
Appearance Colorless to pale-yellow to yellow-brown liquid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿10,500.00
inventory 1g
10-20 days ฿3,260.00

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(R)-Methyl 2,3-dihydroxypropanoate
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(R)-Methyl 2,3-dihydroxypropanoate is a chiral building block primarily utilized in the synthesis of pharmaceutical intermediates, particularly for antiviral nucleoside analogs and other enantiomerically pure compounds. Its (R)-configuration and dihydroxy functionality enable asymmetric synthesis routes to biologically active molecules, such as those used in carbohydrate chemistry and drug development for infectious diseases. It also serves as a precursor in fine chemicals and agrochemicals, where stereo

(R)-Methyl 2,3-dihydroxypropanoate is a chiral building block primarily utilized in the synthesis of pharmaceutical intermediates, particularly for antiviral nucleoside analogs and other enantiomerically pure compounds. Its (R)-configuration and dihydroxy functionality enable asymmetric synthesis routes to biologically active molecules, such as those used in carbohydrate chemistry and drug development for infectious diseases. It also serves as a precursor in fine chemicals and agrochemicals, where stereospecificity is critical for efficacy. In organic synthesis, it is employed to construct complex structures with high purity, contributing to advanced materials and specialty applications.

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