R-(-)-1-Benzyloxy-2-propanol

95%

Reagent Code: #229843
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CAS Number 89401-28-5

science Other reagents with same CAS 89401-28-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.22 g/mol
Formula C₆H₅CH₂OCH₂CH(OH)CH₃
badge Registry Numbers
MDL Number MFCD07367007
inventory_2 Storage & Handling
Density 1.027 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it helps control stereochemistry in complex molecules. Also employed in the preparation of chiral ligands and catalysts for enantioselective reactions. Commonly utilized in research and development for drug discovery due to its functional group compatibility and ease of transformation into target structures.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,160.00
5g
10-20 days ฿2,690.00
10g
10-20 days ฿4,790.00
25g
10-20 days ฿10,360.00
100g
10-20 days ฿40,000.00
R-(-)-1-Benzyloxy-2-propanol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it helps control stereochemistry in complex molecules. Also employed in the preparation of chiral ligands and catalysts for enantioselective reactions. Commonly utilized in research and development for drug discovery due to its functional group compatibility and ease of transformation i

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it helps control stereochemistry in complex molecules. Also employed in the preparation of chiral ligands and catalysts for enantioselective reactions. Commonly utilized in research and development for drug discovery due to its functional group compatibility and ease of transformation into target structures.

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