58885-58-8 | 3-(Boc-amino)-1-propanol

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$7.00	$5.00
5g	97%	in stock	$9.00	$6.00
10g	97%	in stock	$11.00	$8.00
25g	97%	in stock	$26.00	$18.00
100g	>97%	in stock	$70.00	$49.00
500g	97%	in stock	$194.00	$136.00

Description

• Catalog Number: AI53176
• Chemical Name: 3-(Boc-amino)-1-propanol
• CAS Number: 58885-58-8
• Molecular Formula: C8H17NO3
• Molecular Weight: 175.2255
• MDL Number: MFCD00191883
• SMILES: OCCCNC(=O)OC(C)(C)C

Computed Properties

• Complexity: 140
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5
• XLogP3: 0.6

Upstream Synthesis Route

N-Boc-3-aminopropanol, also known as tert-butoxycarbonyl-3-aminopropanol, is a versatile compound commonly used in chemical synthesis. It serves as a valuable building block in organic chemistry due to its ability to undergo various reactions and form a wide array of functionalized products.One key application of N-Boc-3-aminopropanol lies in its use as a protecting group in peptide synthesis. By selectively masking the amino group with the Boc (tert-butoxycarbonyl) protecting group, chemists can control the reactivity of the amino functionality, allowing for specific manipulations elsewhere in the molecule without affecting the protected amine. This protection strategy ensures the desired chemical transformations occur at the intended sites, leading to the synthesis of complex peptides with high efficiency and precision.Moreover, N-Boc-3-aminopropanol can also serve as a precursor for the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Its straightforward functionalization and compatibility with a wide range of synthetic methods make it a valuable intermediate in the preparation of structurally diverse molecules with biological activities or industrial applications.In summary, the strategic incorporation of N-Boc-3-aminopropanol in chemical synthesis enables chemists to streamline complex reactions, access novel molecules, and advance the synthesis of biologically active compounds and materials. Its versatility and reliability make it a vital component in the toolkit of synthetic chemists seeking to develop innovative and efficient synthetic routes.