(1-methylpyrrolidin-3-yl)methanol

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Reagent Code: #208167
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CAS Number 5021-33-0

science Other reagents with same CAS 5021-33-0

blur_circular Chemical Specifications

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Weight 115.18 g/mol
Formula C₆H₁₃NO
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MDL Number MFCD08059753
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) targeting central nervous system disorders. Its structure supports the development of compounds with neurological activity, including potential use in antidepressants and antipsychotics. The hydroxyl and tertiary amine groups allow for derivatization and salt formation, enhancing solubility and bioavailability in drug formulations. Also employed in the preparation of chiral building blocks for asymmetric synthesis in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,900.00
inventory 1g
10-20 days ฿10,990.00
(1-methylpyrrolidin-3-yl)methanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) targeting central nervous system disorders. Its structure supports the development of compounds with neurological activity, including potential use in antidepressants and antipsychotics. The hydroxyl and tertiary amine groups allow for derivatization and salt formation, enhancing solubility and bioavailability in drug formulations. Also employed in the preparation of

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) targeting central nervous system disorders. Its structure supports the development of compounds with neurological activity, including potential use in antidepressants and antipsychotics. The hydroxyl and tertiary amine groups allow for derivatization and salt formation, enhancing solubility and bioavailability in drug formulations. Also employed in the preparation of chiral building blocks for asymmetric synthesis in medicinal chemistry.

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