(S)-2-(Benzylamino)pentanedioic acid

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Reagent Code: #233542
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CAS Number 77539-18-5

science Other reagents with same CAS 77539-18-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.25 g/mol
Formula C₁₂H₁₅NO₄
badge Registry Numbers
MDL Number MFCD00797917
thermostat Physical Properties
Melting Point 160-162 °C
Boiling Point 434.0±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.270±0.06 g/cm3(Predicted)
Storage Room temperature, away from light, dry

description Product Description

Used in pharmaceutical research as a chiral building block for synthesizing neuroactive compounds. Shows potential in the development of drugs targeting glutamate receptors due to structural similarity to endogenous amino acids involved in neurotransmission. Also employed in asymmetric synthesis to introduce stereochemical control in complex molecule construction. Its carboxylic acid groups allow for salt formation and improved solubility in aqueous formulations, making it suitable for early-stage drug screening.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,830.00
inventory 1g
10-20 days ฿4,940.00
inventory 5g
10-20 days ฿17,290.00

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(S)-2-(Benzylamino)pentanedioic acid
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Used in pharmaceutical research as a chiral building block for synthesizing neuroactive compounds. Shows potential in the development of drugs targeting glutamate receptors due to structural similarity to endogenous amino acids involved in neurotransmission. Also employed in asymmetric synthesis to introduce stereochemical control in complex molecule construction. Its carboxylic acid groups allow for salt formation and improved solubility in aqueous formulations, making it suitable for early-stage drug s

Used in pharmaceutical research as a chiral building block for synthesizing neuroactive compounds. Shows potential in the development of drugs targeting glutamate receptors due to structural similarity to endogenous amino acids involved in neurotransmission. Also employed in asymmetric synthesis to introduce stereochemical control in complex molecule construction. Its carboxylic acid groups allow for salt formation and improved solubility in aqueous formulations, making it suitable for early-stage drug screening.

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