(R)-(−)-Benzoin

98%

Reagent Code: #231946
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CAS Number 5928-66-5

science Other reagents with same CAS 5928-66-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.24 g/mol
Formula C₁₄H₁₂O₂
badge Registry Numbers
MDL Number MFCD00082818
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral auxiliary and building block in asymmetric synthesis, particularly in pharmaceuticals and fine chemicals. Its hydroxyl and carbonyl functional groups allow for diverse transformations, such as oxidation, reduction, and condensation reactions. Commonly employed in the preparation of optically active compounds, including intermediates for drugs and natural products. Also serves as a catalyst precursor in certain organocatalytic reactions. Its rigid structure and stereochemistry make it valuable for inducing chirality in carbon-carbon bond-forming reactions.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿3,720.00
inventory 25mg
10-20 days ฿9,990.00
inventory 100mg
10-20 days ฿26,990.00
(R)-(−)-Benzoin
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Used as a chiral auxiliary and building block in asymmetric synthesis, particularly in pharmaceuticals and fine chemicals. Its hydroxyl and carbonyl functional groups allow for diverse transformations, such as oxidation, reduction, and condensation reactions. Commonly employed in the preparation of optically active compounds, including intermediates for drugs and natural products. Also serves as a catalyst precursor in certain organocatalytic reactions. Its rigid structure and stereochemistry make it val

Used as a chiral auxiliary and building block in asymmetric synthesis, particularly in pharmaceuticals and fine chemicals. Its hydroxyl and carbonyl functional groups allow for diverse transformations, such as oxidation, reduction, and condensation reactions. Commonly employed in the preparation of optically active compounds, including intermediates for drugs and natural products. Also serves as a catalyst precursor in certain organocatalytic reactions. Its rigid structure and stereochemistry make it valuable for inducing chirality in carbon-carbon bond-forming reactions.

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