(S)-Methyl morpholine-2-carboxylate hydrochloride

95%

Reagent Code: #234952
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CAS Number 1417789-45-7

science Other reagents with same CAS 1417789-45-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.62 g/mol
Formula C₆H₁₂ClNO₃
thermostat Physical Properties
Boiling Point 349.9±22.0°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral building block in organic synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure compounds. It serves as an intermediate in the synthesis of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in drug efficacy and safety. Its structure allows for selective reactions in asymmetric synthesis, making it valuable in the development of complex molecules. Commonly employed in peptide coupling and as a reagent in nucleoside and nucleotide chemistry. Also utilized in the preparation of catalysts and ligands for stereoselective transformations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿870.00

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(S)-Methyl morpholine-2-carboxylate hydrochloride
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Used as a chiral building block in organic synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure compounds. It serves as an intermediate in the synthesis of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in drug efficacy and safety. Its structure allows for selective reactions in asymmetric synthesis, making it valuable in the development of complex molecules. Commonly employed in peptide coupling and as a reagent in nucl

Used as a chiral building block in organic synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure compounds. It serves as an intermediate in the synthesis of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in drug efficacy and safety. Its structure allows for selective reactions in asymmetric synthesis, making it valuable in the development of complex molecules. Commonly employed in peptide coupling and as a reagent in nucleoside and nucleotide chemistry. Also utilized in the preparation of catalysts and ligands for stereoselective transformations.

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