71989-35-0 | Fmoc-Thr(tBu)-OH

Packsize	Purity	Availability	Price	Discounted Price
5g	99%	in stock	$8.00	$5.00
10g	99%	in stock	$12.00	$8.00
25g	99%	in stock	$23.00	$16.00
100g	99%	in stock	$73.00	$51.00

Description

• Catalog Number: AB46184
• Chemical Name: Fmoc-Thr(tBu)-OH
• CAS Number: 71989-35-0
• Molecular Formula: C23H27NO5
• Molecular Weight: 397.4642
• MDL Number: MFCD00077075
• SMILES: O=C(N[C@@H]([C@H](OC(C)(C)C)C)C(=O)O)OCC1c2ccccc2c2c1cccc2

Computed Properties

• Complexity: 564
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 29
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 8
• XLogP3: 4

Upstream Synthesis Route

(2S,3R)-2-(((9-Fluorenylmethoxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid is a versatile compound widely used in chemical synthesis processes. Known for its unique stereochemistry and functional groups, this compound plays a crucial role in peptide synthesis and modification.In peptide chemistry, (2S,3R)-2-(((9-Fluorenylmethoxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid serves as a key building block for creating peptide chains. Its amino and carboxylic acid groups enable it to participate in peptide bond formation, leading to the development of diverse peptide structures.Additionally, the tert-butoxy and fluorenylmethoxy carbonyl (Fmoc) protecting groups present in this compound offer strategic protection and selective deprotection during peptide assembly. These groups assist in controlling the reactivity and specificity of chemical reactions, allowing for precise manipulation of peptide sequences.Moreover, the (2S,3R) stereochemistry of this compound imparts chirality, making it valuable in the synthesis of enantiopure compounds. By incorporating (2S,3R)-2-(((9-Fluorenylmethoxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid into chemical reactions, chemists can access chiral motifs essential for pharmaceuticals, agrochemicals, and materials science.Overall, (2S,3R)-2-(((9-Fluorenylmethoxy)carbonyl)amino)-3-(tert-butoxy)butanoic acid serves as a fundamental building block in chemical synthesis, facilitating the creation of complex molecules with tailored functionalities and stereochemistries. Its strategic role in peptide chemistry and chiral synthesis makes it a valuable tool for researchers and synthetic chemists striving to develop innovative compounds.