1152113-30-8 | Trans-1-Boc-3-amino-4-methylpyrrolidine

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$167.00	$117.00
250mg	95%	in stock	$333.00	$233.00
500mg	95%	in stock	$638.00	$447.00

Description

• Catalog Number: AA21111
• Chemical Name: Trans-1-Boc-3-amino-4-methylpyrrolidine
• CAS Number: 1152113-30-8
• Molecular Formula: C10H20N2O2
• Molecular Weight: 200.278
• MDL Number: MFCD18375162
• SMILES: N[C@H]1CN(C[C@@H]1C)C(=O)OC(C)(C)C

Computed Properties

• Complexity: 223
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 0.8

Upstream Synthesis Route

The compound (3R,4S)-rel-tert-Butyl 3-amino-4-methylpyrrolidine-1-carboxylate, also known as $name$, plays a crucial role in chemical synthesis due to its unique stereochemistry and functional groups. This compound is commonly utilized as a chiral building block in the synthesis of complex organic molecules. Its 3R and 4S configuration imparts specific stereochemical properties that are essential for creating enantiomerically pure compounds.In chemical synthesis, (3R,4S)-rel-tert-Butyl 3-amino-4-methylpyrrolidine-1-carboxylate serves as a versatile intermediate for constructing bioactive molecules, pharmaceuticals, and agrochemicals. By incorporating this compound into multi-step synthesis routes, chemists can control the chirality and molecular structure of the final product, thus influencing its biological activity and properties.Furthermore, the tert-butyl group on the amino acid side chain provides steric hindrance and can be selectively modified to introduce various functional groups or protective groups. This flexibility allows for tailored modifications during the synthetic process, enabling the creation of diverse chemical entities with specific applications.Overall, the strategic use of (3R,4S)-rel-tert-Butyl 3-amino-4-methylpyrrolidine-1-carboxylate in chemical synthesis facilitates the efficient construction of complex molecules with defined stereochemistry, making it an indispensable tool for organic chemists striving to innovate and design novel compounds.