26250-84-0 | Boc-L-pipecolic acid

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$7.00	$5.00
10g	98%	in stock	$12.00	$9.00
25g	98%	in stock	$24.00	$17.00
100g	98%	in stock	$95.00	$67.00
500g	98%	in stock	$474.00	$332.00

Description

• Catalog Number: AB56033
• Chemical Name: Boc-L-pipecolic acid
• CAS Number: 26250-84-0
• Molecular Formula: C11H19NO4
• Molecular Weight: 229.2729
• MDL Number: MFCD00151904
• SMILES: OC(=O)[C@@H]1CCCCN1C(=O)OC(C)(C)C

Computed Properties

• Complexity: 282
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 1.8

Upstream Synthesis Route

Boc-Pip-OH, also known as tert-butoxycarbonyl-L-pipecolic acid, is a versatile compound widely used in chemical synthesis, particularly in the field of peptide and pharmaceutical chemistry. This compound serves as a key building block due to its ability to protect the amino group in amino acids.In chemical synthesis, Boc-Pip-OH is utilized as a Boc-protected derivative of pipecolic acid, providing a strategic way to control the reactivity of the amino group. By incorporating this compound into the synthetic pathway, chemists can selectively modify specific functional groups while keeping the amino group protected.The application of Boc-Pip-OH extends to the synthesis of peptide structures, where precise control over amino group protection is crucial for stepwise assembly of amino acids. This compound allows for efficient and selective deprotection under mild conditions, enabling the synthesis of complex peptides with high purity and yield.Furthermore, Boc-Pip-OH finds utility in the preparation of various pharmaceutical intermediates and bioactive compounds. Its compatibility with a wide range of chemical reactions makes it a valuable tool for synthetic chemists aiming to construct diverse molecular scaffolds with tailored functionalities.Overall, the strategic use of Boc-Pip-OH in chemical synthesis showcases its significance as a versatile building block in the creation of complex molecules, peptides, and pharmaceuticals.