73-22-3 | H-Trp-OH

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$6.00	$4.00
10g	98%	in stock	$8.00	$5.00
100g	98%	in stock	$10.00	$7.00

Description

• Catalog Number: AB74995
• Chemical Name: H-Trp-OH
• CAS Number: 73-22-3
• Molecular Formula: C11H12N2O2
• Molecular Weight: 204.22518
• MDL Number: MFCD00079394
• SMILES: OC(=O)[C@H](Cc1c[nH]c2c1cccc2)N
• NSC Number: 757373

Computed Properties

• Complexity: 245
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 3
• XLogP3: -1.1

Upstream Synthesis Route

L-Tryptophan, an essential amino acid, serves as a versatile building block in chemical synthesis due to its unique structural characteristics. In the realm of organic chemistry, L-Tryptophan plays a crucial role in the synthesis of various pharmaceutical compounds, agrochemicals, and specialty chemicals. Its aromatic indole ring and functional groups make it an ideal precursor for the preparation of complex molecules through diverse chemical transformations.The indole moiety of L-Tryptophan is particularly valuable in the synthesis of indole alkaloids, a class of natural products with significant biological activities. By utilizing L-Tryptophan as a starting material, chemists can access a wide range of indole derivatives through functional group manipulations, cyclization reactions, and diversification strategies. These indole-based compounds find applications in drug discovery, material science, and bioorganic chemistry, showcasing the importance of L-Tryptophan in contemporary chemical research and development.Moreover, L-Tryptophan's role extends beyond pure organic synthesis, as it serves as a key intermediate in the production of various biochemical compounds and chiral building blocks. Its stereochemical configuration and reactivity enable efficient incorporation into complex molecules with high enantioselectivity, making it a valuable tool for synthetic chemists aiming to access structurally diverse and biologically active compounds.Overall, the versatility and utility of L-Tryptophan in chemical synthesis underscore its significance as a fundamental building block for crafting intricate molecules with tailored properties and functionalities.