(R)-2-(Prop-2-yn-1-yl)pyrrolidine-2-carboxylic acid hydrochloride
97%
- Product Code: 37501
CAS:
1049733-10-9
| Molecular Weight: | 189.64 g./mol | Molecular Formula: | C₈H₁₂ClNO₂ |
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| EC Number: | MDL Number: | MFCD06659239 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(R)-2-(Prop-2-yn-1-yl)pyrrolidine-2-carboxylic acid hydrochloride is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring a pyrrolidine ring and a propargyl group, makes it a valuable building block for developing molecules with potential biological activity. This compound is often utilized in the design and synthesis of enzyme inhibitors, particularly those targeting proteases or other enzymes involved in disease pathways. Additionally, it serves as a precursor in the creation of chiral molecules, which are essential for producing enantiomerically pure drugs, ensuring higher specificity and reduced side effects in therapeutic applications. Its hydrochloride form enhances solubility, making it more suitable for use in aqueous reaction conditions during drug development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $379.14 |
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| 0.250 | 10-20 days | $568.50 |
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| 1.000 | 10-20 days | $1,420.61 |
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(R)-2-(Prop-2-yn-1-yl)pyrrolidine-2-carboxylic acid hydrochloride
(R)-2-(Prop-2-yn-1-yl)pyrrolidine-2-carboxylic acid hydrochloride is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring a pyrrolidine ring and a propargyl group, makes it a valuable building block for developing molecules with potential biological activity. This compound is often utilized in the design and synthesis of enzyme inhibitors, particularly those targeting proteases or other enzymes involved in disease pathways. Additionally, it serves as a precursor in the creation of chiral molecules, which are essential for producing enantiomerically pure drugs, ensuring higher specificity and reduced side effects in therapeutic applications. Its hydrochloride form enhances solubility, making it more suitable for use in aqueous reaction conditions during drug development processes.
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