(1R)-(-)-Menthyl glyoxylate hydrate

97%(HPLC) 

Reagent Code: #230694
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CAS Number 26315-61-7

science Other reagents with same CAS 26315-61-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.29 g/mol
Formula C₁₂H₂₀O₃
thermostat Physical Properties
Melting Point 76-78℃
Boiling Point 95-96℃ 0.3mm
inventory_2 Storage & Handling
Density 1,182 g/cm3
Storage 2-8℃

description Product Description

Used primarily in asymmetric synthesis, this compound serves as a chiral auxiliary in the preparation of enantiomerically pure substances. Its structure allows for high stereoselectivity in reactions such as aldol condensations and alkylations, making it valuable in the synthesis of complex natural products and pharmaceutical intermediates. It is particularly effective in Evans-type oxazolidinone chemistry, where it helps control the formation of new stereocenters. Additionally, it has been employed in the development of fragrances and flavor compounds due to its terpene-derived backbone, contributing to mint-like olfactory profiles in certain aroma chemicals.

Available Sizes & Pricing

Size Availability Unit Price Quantity
200mg
10-20 days ฿10,250.00
(1R)-(-)-Menthyl glyoxylate hydrate
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Used primarily in asymmetric synthesis, this compound serves as a chiral auxiliary in the preparation of enantiomerically pure substances. Its structure allows for high stereoselectivity in reactions such as aldol condensations and alkylations, making it valuable in the synthesis of complex natural products and pharmaceutical intermediates. It is particularly effective in Evans-type oxazolidinone chemistry, where it helps control the formation of new stereocenters. Additionally, it has been employed in t

Used primarily in asymmetric synthesis, this compound serves as a chiral auxiliary in the preparation of enantiomerically pure substances. Its structure allows for high stereoselectivity in reactions such as aldol condensations and alkylations, making it valuable in the synthesis of complex natural products and pharmaceutical intermediates. It is particularly effective in Evans-type oxazolidinone chemistry, where it helps control the formation of new stereocenters. Additionally, it has been employed in the development of fragrances and flavor compounds due to its terpene-derived backbone, contributing to mint-like olfactory profiles in certain aroma chemicals.

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