trans-Methyl 4-methylpyrrolidine-3-carboxylate hydrochloride

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Reagent Code: #51703
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CAS Number 1065065-28-2

science Other reagents with same CAS 1065065-28-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.64 g/mol
Formula C₇H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD30478672
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure is particularly valuable in the development of compounds with potential therapeutic effects, such as inhibitors or modulators of biological targets. Additionally, it is employed in research settings to study the stereochemistry and reactivity of pyrrolidine derivatives, which are important in drug design and development. The hydrochloride form enhances its stability and solubility, making it suitable for use in various chemical reactions and formulations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,464.00

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trans-Methyl 4-methylpyrrolidine-3-carboxylate hydrochloride
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This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure is particularly valuable in the development of compounds with potential therapeutic effects, such as inhibitors or modulators of biological targets. Additionally, it is employed in research settings to study the stereochemistry and reactivity of pyrrolidine derivatives, which are important in drug design and development. The hydrochloride

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure is particularly valuable in the development of compounds with potential therapeutic effects, such as inhibitors or modulators of biological targets. Additionally, it is employed in research settings to study the stereochemistry and reactivity of pyrrolidine derivatives, which are important in drug design and development. The hydrochloride form enhances its stability and solubility, making it suitable for use in various chemical reactions and formulations.

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