Methyl 2-amino-3-hydroxybutanoate hydrochloride

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Reagent Code: #54183
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CAS Number 62076-66-8

science Other reagents with same CAS 62076-66-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.61 g/mol
Formula C₅H₁₂ClNO₃
badge Registry Numbers
MDL Number MFCD00070400
thermostat Physical Properties
Boiling Point 274.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, store under inert gas

description Product Description

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various drugs, particularly those targeting neurological and cardiovascular conditions. Its structure is valuable in the development of chiral molecules, which are crucial for creating enantiomerically pure medications. Additionally, it finds application in organic synthesis for constructing complex molecules with specific stereochemistry, aiding in the production of bioactive compounds and fine chemicals.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿2,700.00
inventory 5g
10-20 days ฿1,629.00
inventory 1g
10-20 days ฿837.00
inventory 25g
10-20 days ฿5,265.00

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Methyl 2-amino-3-hydroxybutanoate hydrochloride
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various drugs, particularly those targeting neurological and cardiovascular conditions. Its structure is valuable in the development of chiral molecules, which are crucial for creating enantiomerically pure medications. Additionally, it finds application in organic synthesis for constructing complex molecules with specific stereochemistry, aiding in the production of bioactive compounds and fine chem

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various drugs, particularly those targeting neurological and cardiovascular conditions. Its structure is valuable in the development of chiral molecules, which are crucial for creating enantiomerically pure medications. Additionally, it finds application in organic synthesis for constructing complex molecules with specific stereochemistry, aiding in the production of bioactive compounds and fine chemicals.

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