1207044-25-4 | 2-[2-({[(tert-butoxy)carbonyl]amino}methyl)-1H-1,3-benzodiazol-1-yl]acetic acid

Packsize	Purity	Availability	Price	Discounted Price
1mg	95%	2 weeks	$574.00	$402.00
5mg	95%	2 weeks	$639.00	$447.00
10mg	95%	2 weeks	$685.00	$479.00
25mg	95%	2 weeks	$850.00	$595.00
50mg	95%	2 weeks	$1,194.00	$836.00
100mg	95%	2 weeks	$1,654.00	$1,158.00
1g	95%	2 weeks	$2,563.00	$1,794.00

Description

• Catalog Number: AV80613
• Chemical Name: 2-[2-({[(tert-butoxy)carbonyl]amino}methyl)-1H-1,3-benzodiazol-1-yl]acetic acid
• CAS Number: 1207044-25-4
• Molecular Formula: C15H19N3O4
• Molecular Weight: 305.3291
• MDL Number: MFCD16640725
• SMILES: OC(=O)Cn1c(CNC(=O)OC(C)(C)C)nc2c1cccc2

Upstream Synthesis Route

The compound $name$ is a key reagent in chemical synthesis due to its versatile applications in various reactions. It serves as a valuable building block in the synthesis of complex organic molecules through its unique structural features. Specifically, the (2-{[(tert-butoxycarbonyl)amino]methyl}-1H-benzimidazol-1-yl)acetic acid moiety plays a crucial role in introducing specific functionalities and structural motifs in the target molecules.In chemical synthesis, $name$ can be used as a protecting group for the amine functionality, allowing selective reactions at other sites without affecting the amine group. This property is particularly valuable in multi-step synthesis where the presence of multiple reactive groups must be carefully managed. Additionally, the benzimidazole ring in $name$ can act as a directing group for selective bond formation, enabling regioselective and stereoselective reactions to take place.Furthermore, the acetic acid moiety in $name$ can serve as a linker for attaching other molecular fragments or modifying the compound's solubility and reactivity. This flexibility enables chemists to design and execute intricate synthetic pathways for the construction of diverse organic compounds.Overall, the strategic incorporation of (2-{[(tert-butoxycarbonyl)amino]methyl}-1H-benzimidazol-1-yl)acetic acid in chemical synthesis offers researchers a powerful tool for designing and executing complex molecular transformations with precision and efficiency.