119397-06-7 | (+)-2-Amino-2-(4-bromophenyl)acetic acid

Packsize	Purity	Availability	Price	Discounted Price
1mg	95%	2 weeks	$284.00	$199.00
5mg	95%	2 weeks	$303.00	$212.00
500mg	95%	2 weeks	$311.00	$218.00
1g	95%	2 weeks	$374.00	$262.00
5g	95%	2 weeks	$706.00	$494.00
10g	95%	2 weeks	$1,038.00	$727.00

Description

• Catalog Number: AE20138
• Chemical Name: (+)-2-Amino-2-(4-bromophenyl)acetic acid
• CAS Number: 119397-06-7
• Molecular Formula: C8H8BrNO2
• Molecular Weight: 230.0586
• MDL Number: MFCD00049327
• SMILES: C1=CC(=CC=C1C(C(=O)O)N)Br

Upstream Synthesis Route

(+)-2-Amino-2-(4-bromophenyl)acetic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis as a key intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Due to its unique chemical structure and functional groups, this compound serves as a crucial building block in various reactions and transformations in organic synthesis.In chemical synthesis, (+)-2-Amino-2-(4-bromophenyl)acetic acid is commonly employed for the preparation of diverse target molecules through processes such as amide formation, esterification, Suzuki coupling, and nucleophilic substitution reactions. Its presence of an amino group and a halogen substituent on the aromatic ring offers opportunities for selective modifications and derivatizations, facilitating the creation of complex molecular structures with specific desired properties.Moreover, the chiral nature of this compound, often available as a single enantiomer, enables stereochemical control in asymmetric synthesis, leading to the creation of optically active compounds with potential biological activities or improved efficacy. The incorporation of (+)-2-Amino-2-(4-bromophenyl)acetic acid into synthetic pathways allows chemists to access structurally diverse compounds with tailored functionalities, offering a powerful tool for the discovery and development of novel chemical entities across various industries.