(S)-2-Amino-3-(benzo[d][1,3]dioxol-4-yl)propanoic acid hydrochloride

95%

Reagent Code: #233239
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CAS Number 2563272-51-3

science Other reagents with same CAS 2563272-51-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.66 g/mol
Formula C₁₀H₁₂ClNO₄
badge Registry Numbers
MDL Number MFCD32062603
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in pharmaceutical research as a chiral building block for synthesizing neuroactive compounds. Shows potential in the development of agents targeting central nervous system disorders due to its structural similarity to natural amino acids involved in neurotransmission. Also employed in studies related to dopamine and serotonin pathways because of the benzodioxole moiety, which is known for interacting with neuronal receptors. Commonly utilized in asymmetric synthesis and medicinal chemistry for optimizing drug candidates with improved selectivity and metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,050.00
inventory 250mg
10-20 days ฿33,020.00
(S)-2-Amino-3-(benzo[d][1,3]dioxol-4-yl)propanoic acid hydrochloride
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Used in pharmaceutical research as a chiral building block for synthesizing neuroactive compounds. Shows potential in the development of agents targeting central nervous system disorders due to its structural similarity to natural amino acids involved in neurotransmission. Also employed in studies related to dopamine and serotonin pathways because of the benzodioxole moiety, which is known for interacting with neuronal receptors. Commonly utilized in asymmetric synthesis and medicinal chemistry for optim

Used in pharmaceutical research as a chiral building block for synthesizing neuroactive compounds. Shows potential in the development of agents targeting central nervous system disorders due to its structural similarity to natural amino acids involved in neurotransmission. Also employed in studies related to dopamine and serotonin pathways because of the benzodioxole moiety, which is known for interacting with neuronal receptors. Commonly utilized in asymmetric synthesis and medicinal chemistry for optimizing drug candidates with improved selectivity and metabolic stability.

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