(S)-5-BOC-5-AZASPIRO[2.4]HEPTANE-6-CARBOXYLIC ACID METHYL ESTER

95%

Reagent Code: #74785
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CAS Number 1129634-43-0

science Other reagents with same CAS 1129634-43-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255 g/mol
Formula C₁₃H₂₁NO₄
badge Registry Numbers
MDL Number MFCD25541909
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its spirocyclic structure and functional groups make it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological disorders and other therapeutic areas. The BOC (tert-butoxycarbonyl) protecting group allows for selective reactions during multi-step synthetic processes, ensuring the integrity of the molecule. Additionally, the methyl ester moiety can be hydrolyzed or transformed into other functional groups, enhancing its versatility in medicinal chemistry. Its application is crucial in the preparation of compounds with potential biological activity, contributing to advancements in drug discovery and development.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿22,250.00
inventory 1g
10-20 days ฿61,560.00

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(S)-5-BOC-5-AZASPIRO[2.4]HEPTANE-6-CARBOXYLIC ACID METHYL ESTER
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This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its spirocyclic structure and functional groups make it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological disorders and other therapeutic areas. The BOC (tert-butoxycarbonyl) protecting group allows for selective reactions during multi-step synthetic processes, ensuring the integrity of the

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its spirocyclic structure and functional groups make it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological disorders and other therapeutic areas. The BOC (tert-butoxycarbonyl) protecting group allows for selective reactions during multi-step synthetic processes, ensuring the integrity of the molecule. Additionally, the methyl ester moiety can be hydrolyzed or transformed into other functional groups, enhancing its versatility in medicinal chemistry. Its application is crucial in the preparation of compounds with potential biological activity, contributing to advancements in drug discovery and development.

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