142356-33-0 | N-Boc-6-bromo-hexylamine

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$8.00	$5.00
1g	97%	in stock	$13.00	$9.00
5g	97%	in stock	$40.00	$28.00
10g	97%	in stock	$75.00	$52.00

Description

• Catalog Number: AB46710
• Chemical Name: N-Boc-6-bromo-hexylamine
• CAS Number: 142356-33-0
• Molecular Formula: C11H22BrNO2
• Molecular Weight: 280.2019
• MDL Number: MFCD06201019
• SMILES: BrCCCCCCNC(=O)OC(C)(C)C

Computed Properties

• Complexity: 178
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 8
• XLogP3: 3.1

Upstream Synthesis Route

The N-Boc-6-bromohexylamine is a versatile compound commonly employed in chemical synthesis as a valuable building block for the fine chemical and pharmaceutical industries. With its unique structure and functional groups, this compound serves as a key intermediate in the synthesis of various organic compounds with complex structures and diverse functionalities.In chemical synthesis, N-Boc-6-bromohexylamine plays a crucial role as a synthetic precursor for the introduction of the Boc (tert-butyloxycarbonyl) protecting group. This protective group is widely utilized to temporarily mask reactive functional groups and prevent unwanted side reactions during the synthesis of complex molecules. The presence of the Boc group helps in controlling the reactivity and selectivity of subsequent chemical reactions, allowing for precise manipulation of the molecule's structure.Additionally, the bromo substituent in N-Boc-6-bromohexylamine enables further functionalization through cross-coupling reactions, such as Suzuki-Miyaura coupling or Heck reaction, to introduce new chemical moieties into the molecule. This provides chemists with the flexibility to tailor the compound's properties and enhance its potential applications in drug discovery, material science, and agrochemical development.Overall, the strategic incorporation of N-Boc-6-bromohexylamine in chemical synthesis offers synthetic chemists a powerful tool to access structurally complex molecules with precise control over functional group manipulations and property enhancements.