(S)-Butyl 2-aminopropanoate

97%

Reagent Code: #235021
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CAS Number 2885-02-1

science Other reagents with same CAS 2885-02-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 145.2 g/mol
Formula C₇H₁₅NO₂
badge Registry Numbers
MDL Number MFCD12796122
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a chiral building block in the synthesis of pharmaceuticals, especially in the production of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its ester functionality allows for easy manipulation in multi-step organic syntheses, making it valuable in creating alpha-amino acids and derivatives. Commonly employed in the development of central nervous system agents and cardiovascular drugs due to its ability to enhance metabolic stability and bioavailability in final drug compounds. Also utilized in asymmetric synthesis to introduce chirality, improving the selectivity and potency of medicinal molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿486.00
inventory 1g
10-20 days ฿1,780.00
inventory 5g
10-20 days ฿7,580.00
(S)-Butyl 2-aminopropanoate
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Used primarily as a chiral building block in the synthesis of pharmaceuticals, especially in the production of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its ester functionality allows for easy manipulation in multi-step organic syntheses, making it valuable in creating alpha-amino acids and derivatives. Commonly employed in the development of central nervous system agents and cardiovascular drugs due to its ability to enhance metabolic stability and bioavailability in fin

Used primarily as a chiral building block in the synthesis of pharmaceuticals, especially in the production of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its ester functionality allows for easy manipulation in multi-step organic syntheses, making it valuable in creating alpha-amino acids and derivatives. Commonly employed in the development of central nervous system agents and cardiovascular drugs due to its ability to enhance metabolic stability and bioavailability in final drug compounds. Also utilized in asymmetric synthesis to introduce chirality, improving the selectivity and potency of medicinal molecules.

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