(S)-tert-Butyl 2-(aminomethyl)pyrrolidine-1-carboxylate hydrochloride
95%
- Product Code: 126382
CAS:
1190890-11-9
Molecular Weight: | 236.74 g./mol | Molecular Formula: | C10H21ClN2O2 |
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EC Number: | MDL Number: | MFCD11101392 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily used in pharmaceutical research and development as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a pyrrolidine ring and a protected amine group, makes it valuable in the preparation of compounds with potential biological activity, particularly in the fields of neuroscience and oncology. It is often employed in asymmetric synthesis to create enantiomerically pure molecules, which are crucial for developing drugs with high specificity and reduced side effects. Additionally, it serves as an intermediate in the production of peptidomimetics and other bioactive molecules, contributing to advancements in drug discovery and medicinal chemistry.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿2,400.00 |
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0.250 | 10-20 days | ฿5,950.00 |
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1.000 | 10-20 days | ฿23,750.00 |
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(S)-tert-Butyl 2-(aminomethyl)pyrrolidine-1-carboxylate hydrochloride
This compound is primarily used in pharmaceutical research and development as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a pyrrolidine ring and a protected amine group, makes it valuable in the preparation of compounds with potential biological activity, particularly in the fields of neuroscience and oncology. It is often employed in asymmetric synthesis to create enantiomerically pure molecules, which are crucial for developing drugs with high specificity and reduced side effects. Additionally, it serves as an intermediate in the production of peptidomimetics and other bioactive molecules, contributing to advancements in drug discovery and medicinal chemistry.
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