string(7) "reagent" Dimethyl (S)-2-methoxysuccinate

Dimethyl (S)-2-methoxysuccinate

95%

Reagent Code: #233503
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CAS Number 27871-50-7

science Other reagents with same CAS 27871-50-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.17 g/mol
Formula C₇H₁₂O₅
thermostat Physical Properties
Boiling Point 223.4±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.116±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a chiral building block in pharmaceutical synthesis, particularly in the production of active pharmaceutical ingredients (APIs) where stereochemistry is critical. Its ester groups allow for easy modification and incorporation into larger molecules, making it valuable in asymmetric synthesis. Commonly employed in the development of protease inhibitors and other bioactive compounds due to its ability to mimic natural metabolites. Also utilized in the preparation of intermediates for antiviral and antitumor agents. Its methoxy group enhances solubility and can influence the metabolic stability of the final drug product.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,100.00
inventory 250mg
10-20 days ฿7,010.00
inventory 1g
10-20 days ฿18,890.00

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Dimethyl (S)-2-methoxysuccinate
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Used as a chiral building block in pharmaceutical synthesis, particularly in the production of active pharmaceutical ingredients (APIs) where stereochemistry is critical. Its ester groups allow for easy modification and incorporation into larger molecules, making it valuable in asymmetric synthesis. Commonly employed in the development of protease inhibitors and other bioactive compounds due to its ability to mimic natural metabolites. Also utilized in the preparation of intermediates for antiviral and a

Used as a chiral building block in pharmaceutical synthesis, particularly in the production of active pharmaceutical ingredients (APIs) where stereochemistry is critical. Its ester groups allow for easy modification and incorporation into larger molecules, making it valuable in asymmetric synthesis. Commonly employed in the development of protease inhibitors and other bioactive compounds due to its ability to mimic natural metabolites. Also utilized in the preparation of intermediates for antiviral and antitumor agents. Its methoxy group enhances solubility and can influence the metabolic stability of the final drug product.

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