(S)-Isoindoline-1-carboxylic acid hydrochloride

97%

Reagent Code: #235656
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CAS Number 1965314-73-1

science Other reagents with same CAS 1965314-73-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.63 g/mol
Formula C₉H₁₀ClNO₂
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MDL Number MFCD28098115
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the formation of peptidomimetics and heterocyclic compounds, making it valuable in drug discovery for central nervous system agents, protease inhibitors, and other bioactive molecules. Commonly employed in asymmetric synthesis due to its stable stereocenter, facilitating the creation of complex molecules with defined spatial orientation. Also utilized in the preparation of intermediates for agrochemicals and specialty chemicals where stereochemistry plays a critical role in biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,740.00
inventory 250mg
10-20 days ฿17,180.00
inventory 1g
10-20 days ฿42,970.00
(S)-Isoindoline-1-carboxylic acid hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the formation of peptidomimetics and heterocyclic compounds, making it valuable in drug discovery for central nervous system agents, protease inhibitors, and other bioactive molecules. Commonly employed in asymmetric synthesis due to its stable stereocenter, facilitating the creation of complex molecules

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the formation of peptidomimetics and heterocyclic compounds, making it valuable in drug discovery for central nervous system agents, protease inhibitors, and other bioactive molecules. Commonly employed in asymmetric synthesis due to its stable stereocenter, facilitating the creation of complex molecules with defined spatial orientation. Also utilized in the preparation of intermediates for agrochemicals and specialty chemicals where stereochemistry plays a critical role in biological activity.

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