1134328-09-8 | tert-Butyl (3-(methylamino)phenyl)carbamate

Packsize	Purity	Availability	Price	Discounted Price
100mg	96%	in stock	$75.00	$52.00
250mg	96%	in stock	$89.00	$62.00
1g	96%	in stock	$257.00	$180.00
5g	96%	in stock	$976.00	$683.00

Description

• Catalog Number: AA10904
• Chemical Name: tert-Butyl (3-(methylamino)phenyl)carbamate
• CAS Number: 1134328-09-8
• Molecular Formula: C12H18N2O2
• Molecular Weight: 222.2835
• MDL Number: MFCD11858352
• SMILES: CNc1cccc(c1)NC(=O)OC(C)(C)C

Computed Properties

• Complexity: 236
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4
• XLogP3: 2.5

Upstream Synthesis Route

The tert-Butyl (3-(methylamino)phenyl)carbamate, also known as $name$, is a versatile compound widely used in chemical synthesis. With its unique structure and properties, this compound finds application in various reactions and processes in the field of organic chemistry. $name$ is commonly employed as a protecting group in peptide synthesis due to its ability to selectively shield specific functional groups, thus allowing for the targeted manipulation of the molecule. This compound also serves as a valuable reagent in the preparation of pharmaceutical intermediates and bioactive compounds. Its presence can facilitate the formation of complex molecular structures by enabling controlled reactions and strategic derivatization.Furthermore, $name$ plays a crucial role in the field of medicinal chemistry, where it is utilized in the design and synthesis of novel drug candidates. Its compatibility with a wide range of reaction conditions and compatibility with various functional groups make it a valuable tool for medicinal chemists striving to develop therapeutically potent compounds with improved pharmacokinetic profiles.In summary, the tert-Butyl (3-(methylamino)phenyl)carbamate, $name$, is a key component in chemical synthesis, offering diverse applications in peptide synthesis, pharmaceutical development, and medicinal chemistry. Its strategic incorporation in synthetic pathways contributes to the advancement of drug discovery and the creation of specialized organic molecules.