(R)-(−)-N-Benzyl-2-phenylglycinol

98%

Reagent Code: #230640
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CAS Number 14231-57-3

science Other reagents with same CAS 14231-57-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.3 g/mol
Formula C₁₅H₁₇NO
badge Registry Numbers
MDL Number MFCD00674035
thermostat Physical Properties
Boiling Point 386.4 °C at 760mmHg
inventory_2 Storage & Handling
Density 1.1 g/cm3
Storage 2-8°C

description Product Description

Used as a chiral auxiliary and building block in asymmetric synthesis, particularly in the preparation of biologically active compounds. Its stereochemistry enables high enantioselectivity in reactions such as alkylations, cyclizations, and catalytic reductions. Commonly employed in the pharmaceutical industry for synthesizing enantiomerically pure drugs, especially those targeting central nervous system disorders and cardiovascular diseases. Also utilized in the development of chiral ligands for asymmetric catalysis, enhancing the efficiency of metal-catalyzed reactions. Its structural features allow for easy modification and incorporation into complex molecular architectures.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,390.00
5g
10-20 days ฿6,560.00
25g
10-20 days ฿24,050.00
(R)-(−)-N-Benzyl-2-phenylglycinol
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Used as a chiral auxiliary and building block in asymmetric synthesis, particularly in the preparation of biologically active compounds. Its stereochemistry enables high enantioselectivity in reactions such as alkylations, cyclizations, and catalytic reductions. Commonly employed in the pharmaceutical industry for synthesizing enantiomerically pure drugs, especially those targeting central nervous system disorders and cardiovascular diseases. Also utilized in the development of chiral ligands for asymmetric
Used as a chiral auxiliary and building block in asymmetric synthesis, particularly in the preparation of biologically active compounds. Its stereochemistry enables high enantioselectivity in reactions such as alkylations, cyclizations, and catalytic reductions. Commonly employed in the pharmaceutical industry for synthesizing enantiomerically pure drugs, especially those targeting central nervous system disorders and cardiovascular diseases. Also utilized in the development of chiral ligands for asymmetric catalysis, enhancing the efficiency of metal-catalyzed reactions. Its structural features allow for easy modification and incorporation into complex molecular architectures.
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