()-1,4-Di-O-benzyl-D-threitol

98.0%

Reagent Code: #70766
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Alias (+)-1,4-Di-O-benzyl-D-threanol (+)-1,4-O-Diphenyl-D-threol (+)-(2R,3R)-1,4-bis(benzyloxy)-2,3-butanediol (+)-1,4-Di-O-benzyl-D-threitol 1,4-Di-O-benzyl-D-threool
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CAS Number 91604-41-0

science Other reagents with same CAS 91604-41-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.37 g/mol
Formula C₁₈H₂₂O₄
badge Registry Numbers
MDL Number MFCD00077722
thermostat Physical Properties
Melting Point 55-58 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used in organic synthesis as a chiral building block. It is particularly valuable in the preparation of complex molecules, such as pharmaceuticals and natural products, where stereochemical control is essential. The compound serves as a key intermediate in the synthesis of enantiomerically pure substances, enabling the creation of specific stereoisomers with high precision. Its benzyl-protected hydroxyl groups make it suitable for selective deprotection and further functionalization, allowing chemists to tailor its structure for various applications. Additionally, it is employed in the development of ligands for asymmetric catalysis, contributing to the production of optically active compounds in industries like drug manufacturing and fine chemicals.

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Test Parameter Specification
Melting point 56-59
Optical Purity 0-0
Purity (GC) 98-100%
Specific Rotation (20°C, c=5, CHCl3) 6-6.5
APPEARANCE White powder, crystals and/or chunks
Infrared Spectrometry Conforms to Structure
Proton NMR Spectrum Conforms to Structure
Solubility in Chloroform almost transparent

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inventory 1g
10-20 days ฿12,105.00

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()-1,4-Di-O-benzyl-D-threitol
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This chemical is primarily used in organic synthesis as a chiral building block. It is particularly valuable in the preparation of complex molecules, such as pharmaceuticals and natural products, where stereochemical control is essential. The compound serves as a key intermediate in the synthesis of enantiomerically pure substances, enabling the creation of specific stereoisomers with high precision. Its benzyl-protected hydroxyl groups make it suitable for selective deprotection and further functionaliz

This chemical is primarily used in organic synthesis as a chiral building block. It is particularly valuable in the preparation of complex molecules, such as pharmaceuticals and natural products, where stereochemical control is essential. The compound serves as a key intermediate in the synthesis of enantiomerically pure substances, enabling the creation of specific stereoisomers with high precision. Its benzyl-protected hydroxyl groups make it suitable for selective deprotection and further functionalization, allowing chemists to tailor its structure for various applications. Additionally, it is employed in the development of ligands for asymmetric catalysis, contributing to the production of optically active compounds in industries like drug manufacturing and fine chemicals.

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