(S)-2-Amino-2-(2,3-dihydro-1H-inden-2-yl)acetic acid

97%

Reagent Code: #232486
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CAS Number 155239-51-3

science Other reagents with same CAS 155239-51-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.2264 g/mol
Formula C₁₁H₁₃NO₂
badge Registry Numbers
MDL Number MFCD08275743
thermostat Physical Properties
Boiling Point 372.9±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.254±0.06 g/cm3(Predicted)
Storage Room temperature, 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 rigid indane structure provides stereochemical control in asymmetric synthesis, making it valuable for creating enantiomerically pure compounds. Commonly employed in the preparation of nootropic drugs and enzyme inhibitors where stereochemistry influences biological activity. Also utilized in research settings for developing novel bioactive molecules and in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,640.00
inventory 1g
10-20 days ฿52,090.00

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(S)-2-Amino-2-(2,3-dihydro-1H-inden-2-yl)acetic acid
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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 rigid indane structure provides stereochemical control in asymmetric synthesis, making it valuable for creating enantiomerically pure compounds. Commonly employed in the preparation of nootropic drugs and enzyme inhibitors where stereochemistry influences biological activity. Also utilized in research settings for developing novel bioactive molecules and in medicinal

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its rigid indane structure provides stereochemical control in asymmetric synthesis, making it valuable for creating enantiomerically pure compounds. Commonly employed in the preparation of nootropic drugs and enzyme inhibitors where stereochemistry influences biological activity. Also utilized in research settings for developing novel bioactive molecules and in medicinal chemistry for structure-activity relationship studies.

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