(S)-Methyl 3-amino-2,3-dihydro-1H-indene-5-carboxylate hydrochloride

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Reagent Code: #38428
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CAS Number 1246509-66-9

science Other reagents with same CAS 1246509-66-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.69 g/mol
Formula C₁₁H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD22393235
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in pharmaceutical research as an intermediate in the synthesis of more complex molecules, particularly those targeting neurological and cardiovascular diseases. Its structure is valuable for developing drugs that modulate specific receptors or enzymes in the body. Additionally, it is employed in the study of chiral chemistry due to its stereospecific properties, aiding in the creation of enantiomerically pure substances. Researchers also explore its potential in designing novel therapeutic agents with improved efficacy and reduced side effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,293.00
inventory 1g
10-20 days ฿49,986.00
inventory 100mg
10-20 days ฿10,944.00

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(S)-Methyl 3-amino-2,3-dihydro-1H-indene-5-carboxylate hydrochloride
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This compound is primarily utilized in pharmaceutical research as an intermediate in the synthesis of more complex molecules, particularly those targeting neurological and cardiovascular diseases. Its structure is valuable for developing drugs that modulate specific receptors or enzymes in the body. Additionally, it is employed in the study of chiral chemistry due to its stereospecific properties, aiding in the creation of enantiomerically pure substances. Researchers also explore its potential in design

This compound is primarily utilized in pharmaceutical research as an intermediate in the synthesis of more complex molecules, particularly those targeting neurological and cardiovascular diseases. Its structure is valuable for developing drugs that modulate specific receptors or enzymes in the body. Additionally, it is employed in the study of chiral chemistry due to its stereospecific properties, aiding in the creation of enantiomerically pure substances. Researchers also explore its potential in designing novel therapeutic agents with improved efficacy and reduced side effects.

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