112525-72-1 | N-tert-Butoxycarbonyl-D,L-tryptophan

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$6.00	$4.00
5g	97%	in stock	$7.00	$5.00
10g	97%	in stock	$10.00	$7.00
25g	97%	in stock	$14.00	$10.00
100g	97%	in stock	$54.00	$38.00
500g	97%	in stock	$265.00	$186.00

Description

• Catalog Number: AD76123
• Chemical Name: N-tert-Butoxycarbonyl-D,L-tryptophan
• CAS Number: 112525-72-1
• Molecular Formula: C16H20N2O4
• Molecular Weight: 304.3410
• MDL Number: MFCD00190836
• SMILES: O=C(OC(C)(C)C)NC(C(=O)O)Cc1c[nH]c2c1cccc2

Upstream Synthesis Route

2-((tert-Butoxycarbonyl)amino)-3-(1H-indol-3-yl)propanoic acid, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis. In the field of organic chemistry, this compound serves as a valuable building block for the preparation of various pharmaceuticals, natural products, and other complex molecules.One key application of $name$ in chemical synthesis is its use as a protected amino acid derivative. The tert-butoxycarbonyl (Boc) group on the amino moiety provides protection against undesired reactions during subsequent synthetic steps. This protection strategy allows chemists to selectively manipulate other functional groups in the molecule while keeping the amine group intact until needed.Furthermore, the presence of the indole ring in the structure of $name$ confers valuable properties to the compound. Indole derivatives are known for their biological activities and are commonly found in many bioactive molecules. Incorporating the indole moiety into a synthesis route can lead to the generation of compounds with diverse pharmacological properties.Overall, the strategic placement of the Boc-protected amino acid unit and the indole group in the structure of 2-((tert-Butoxycarbonyl)amino)-3-(1H-indol-3-yl)propanoic acid makes it a valuable intermediate in the synthesis of various complex molecules with potential applications in drug discovery and chemical biology.