75937-12-1 | 6-(tert-Butoxycarbonylamino)-1-hexanol

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$13.00	$9.00
1g	97%	in stock	$26.00	$18.00
5g	97%	in stock	$46.00	$33.00
10g	95%	in stock	$89.00	$63.00
25g	≥98%	in stock	$183.00	$128.00

Description

• Catalog Number: AB45358
• Chemical Name: 6-(tert-Butoxycarbonylamino)-1-hexanol
• CAS Number: 75937-12-1
• Molecular Formula: C11H23NO3
• Molecular Weight: 217.3052
• MDL Number: MFCD01862954
• SMILES: OCCCCCCNC(=O)OC(C)(C)C

Computed Properties

• Complexity: 175
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 8
• XLogP3: 1.7

Upstream Synthesis Route

6-(tert-Butoxycarbonylamino)-1-hexanol is a versatile compound commonly used in chemical synthesis due to its unique properties. This compound serves as a valuable building block in organic chemistry, particularly in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its functionality as an amine and alcohol group offers a wide range of opportunities for structural modifications and derivatization, making it a key intermediate in the development of complex molecules. Additionally, the tert-butoxycarbonyl (Boc) protecting group provides stability and facilitates selective reactions, enhancing the efficiency and precision of synthetic routes. Its compatibility with various reagents and reaction conditions makes it a valuable tool for organic chemists seeking to access diverse chemical space and target-specific molecular structures. In summary, 6-(tert-Butoxycarbonylamino)-1-hexanol plays a crucial role in the design and synthesis of advanced chemical compounds with diverse applications in the field of chemistry.

Literature

• Synthesis and g-quadruplex-binding properties of defined acridine oligomers.

  Journal of nucleic acids 20100101