(S)-Ethyl 2-amino-3-(4-chlorophenyl)propanoate hydrochloride

95%

Reagent Code: #236427
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CAS Number 51366-22-4

science Other reagents with same CAS 51366-22-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.151 g/mol
Formula C₁₁H₁₅Cl₂NO₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of both amine and ester functionalities in a stereochemically defined arrangement. Commonly employed in the preparation of antihypertensive and anticonvulsant compounds. Also utilized in asymmetric synthesis to introduce the 4-chlorophenyl moiety with high enantioselectivity. The hydrochloride salt form enhances stability and handling during industrial processing.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,060.00
inventory 5g
10-20 days ฿11,800.00
inventory 1g
10-20 days ฿2,890.00

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(S)-Ethyl 2-amino-3-(4-chlorophenyl)propanoate hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of both amine and ester functionalities in a stereochemically defined arrangement. Commonly employed in the preparation of antihypertensive and anticonvulsant compounds. Also utilized in asymmetric synthesis to introduce the 4-chlorophenyl moiety with high enantioselectivity. The hydrochloride

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of both amine and ester functionalities in a stereochemically defined arrangement. Commonly employed in the preparation of antihypertensive and anticonvulsant compounds. Also utilized in asymmetric synthesis to introduce the 4-chlorophenyl moiety with high enantioselectivity. The hydrochloride salt form enhances stability and handling during industrial processing.

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