100222-98-8 | 6-((tert-Butoxycarbonyl)(methyl)amino)hexanoic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$80.00	$56.00
1g	97%	in stock	$400.00	$280.00
5g	97%	in stock	$1,505.00	$1,053.00

Description

• Catalog Number: AA01457
• Chemical Name: 6-((tert-Butoxycarbonyl)(methyl)amino)hexanoic acid
• CAS Number: 100222-98-8
• Molecular Formula: C12H23NO4
• Molecular Weight: 245.31531999999999
• MDL Number: MFCD24466707
• SMILES: OC(=O)CCCCCN(C(=O)OC(C)(C)C)C

Upstream Synthesis Route

6-((tert-Butoxycarbonyl)(methyl)amino)hexanoic acid is a versatile compound widely employed in chemical synthesis due to its unique properties and reactivity. This compound serves as an important building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its primary application lies in the field of peptide chemistry, where it is utilized as a key intermediate for the synthesis of peptide-based drugs and bioactive compounds.In peptide synthesis, 6-((tert-Butoxycarbonyl)(methyl)amino)hexanoic acid acts as a protecting group for the amino group, allowing selective functionalization of specific amino acids within a peptide chain. This protective group can be easily removed under mild conditions, enabling the sequential assembly of complex peptide sequences with high efficiency and purity.Furthermore, this compound also finds utility in the preparation of chiral building blocks and amino acid derivatives, where its unique structural features contribute to the stereochemical control and regioselectivity of chemical reactions. Its compatibility with a wide range of coupling reagents and activation methods makes it a valuable tool for the synthesis of diverse organic molecules with tailored properties and functionalities.Overall, the application of 6-((tert-Butoxycarbonyl)(methyl)amino)hexanoic acid in chemical synthesis offers researchers and chemists a powerful platform for the design and construction of molecular structures with precision and control. Its versatility, reactivity, and compatibility make it an indispensable tool in modern organic synthesis strategies.