175724-30-8 | tert-Butyl 3,3'-(2-amino-2-((3-tert-butoxy-3-oxopropoxy)methyl)propane-1,3-diyl)bis(oxy)dipropanoate

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$9.00	$6.00
250mg	97%	in stock	$20.00	$14.00
1g	97%	in stock	$35.00	$24.00
5g	97%	in stock	$126.00	$88.00
10g	97%	in stock	$248.00	$173.00
25g	97%	in stock	$480.00	$336.00

Description

• Catalog Number: AA94598
• Chemical Name: tert-Butyl 3,3'-(2-amino-2-((3-tert-butoxy-3-oxopropoxy)methyl)propane-1,3-diyl)bis(oxy)dipropanoate
• CAS Number: 175724-30-8
• Molecular Formula: C25H47NO9
• Molecular Weight: 505.642
• MDL Number: MFCD18252299
• SMILES: O=C(OC(C)(C)C)CCOCC(COCCC(=O)OC(C)(C)C)(COCCC(=O)OC(C)(C)C)N

Computed Properties

• Complexity: 569
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 35
• Hydrogen Bond Acceptor Count: 10
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 21
• XLogP3: 1.2

Upstream Synthesis Route

Tris[[2-(tert-butoxycarbonyl)ethoxy]methyl]methylamine is a versatile compound commonly used in chemical synthesis as a protecting group for amines. This compound plays a crucial role in organic synthesis by temporarily blocking the reactive amine functional groups in molecules, thus allowing selective reactions to occur elsewhere in the molecule. By serving as a protecting group, Tris[[2-(tert-butoxycarbonyl)ethoxy]methyl]methylamine enables chemists to control and manipulate the chemical transformations of amines, leading to the synthesis of complex organic compounds with high precision. Its application in chemical synthesis extends to various industries, including pharmaceuticals, materials science, and agrochemicals, where the creation of specific functional groups is essential for the development of new and advanced compounds.

Literature

• A simple and accessible synthetic lectin for glucose recognition and sensing.

  Nature chemistry 20120901