91419-48-6 | N-BOC-4-Pieridinecarboxamide

Packsize	Purity	Availability	Price	Discounted Price
25g	97%	in stock	$12.00	$9.00
100g	97%	in stock	$47.00	$33.00

Description

• Catalog Number: AC94043
• Chemical Name: N-BOC-4-Pieridinecarboxamide
• CAS Number: 91419-48-6
• Molecular Formula: C11H20N2O3
• Molecular Weight: 228.2881
• MDL Number: MFCD02180953
• SMILES: O=C(N1CCC(CC1)C(=O)N)OC(C)(C)C

Computed Properties

• Complexity: 275
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 0.5

Upstream Synthesis Route

1-Piperidinecarboxylic acid, 4-(aminocarbonyl)-, 1,1-dimethylethyl ester, commonly known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is widely utilized in the pharmaceutical industry for the synthesis of various biologically active molecules. Its unique chemical properties make it an essential component in the development of potential drug candidates.In chemical synthesis, $name$ acts as a key intermediate in the creation of complex organic compounds through different reactions such as acylation, amidation, and alkylation. By incorporating this compound into synthetic pathways, chemists can efficiently introduce the desired functional groups and structural motifs necessary for the development of new pharmaceuticals.Furthermore, the 1,1-dimethylethyl ester group in $name$ provides stability and protection to the molecule during synthetic manipulations, allowing for selective modifications at specific sites. This feature enhances the precision and control of chemical reactions, leading to improved yields and purity of the final product.Overall, the application of 1-Piperidinecarboxylic acid, 4-(aminocarbonyl)-, 1,1-dimethylethyl ester in chemical synthesis underscores its importance as a valuable tool for designing and synthesizing novel compounds with potential therapeutic benefits.

Literature

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501