124443-68-1 | Methyl (1-BOC-piperidin-4-yl)carboxylate

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$15.00	$10.00
10g	98%	in stock	$18.00	$12.00
25g	98%	in stock	$20.00	$14.00
100g	98%	in stock	$22.00	$16.00

Description

• Catalog Number: AA28365
• Chemical Name: Methyl (1-BOC-piperidin-4-yl)carboxylate
• CAS Number: 124443-68-1
• Molecular Formula: C12H21NO4
• Molecular Weight: 243.2994
• MDL Number: MFCD02183584
• SMILES: COC(=O)C1CCN(CC1)C(=O)OC(C)(C)C
• NSC Number: 693923

Computed Properties

• Complexity: 287
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• XLogP3: 1.5

Upstream Synthesis Route

N-Boc-piperidine-4-carboxylic acid methyl ester serves as a versatile building block in chemical synthesis, particularly in the field of organic chemistry. With its characteristic N-Boc protection group and ester functionality, this compound is utilized as a valuable intermediate for the synthesis of various pharmaceuticals, agrochemicals, and other complex organic molecules.In organic synthesis, the N-Boc protection group on the piperidine ring provides a temporary shield for the amine functionality, allowing for selective reactions at other sites within the molecule. By controlling the deprotection of the N-Boc group under specific conditions, chemists can manipulate the reactivity and selectivity of the compound during subsequent synthetic steps.Additionally, the methyl ester moiety offers opportunities for further functionalization through esterification, hydrolysis, or transesterification reactions. This flexibility enables chemists to tailor the structure of the molecule to meet the requirements of a desired target compound, making N-Boc-piperidine-4-carboxylic acid methyl ester a valuable tool in the synthesis of diverse organic molecules.