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189337-28-8

Carbamic acid, N-[(1R,2R)-2-(1,1-dimethylethoxy)-1-(hydroxymethyl)propyl]-, 9H-fluoren-9-ylmethyl ester

Catalog#: AR002J13  |   CAS#: 189337-28-8  |   MDL#: MFCD00235950  |   MF: C23H29NO4  |   MW: 383.4807

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250mg 98% $3.00 Global Stock Buy Now Add To Cart
1g 98% $4.00 Global Stock Buy Now Add To Cart
5g 98% $17.00 Global Stock Buy Now Add To Cart
25g 98% $69.00 Global Stock Buy Now Add To Cart
100g 98% $273.00 Global Stock Buy Now Add To Cart
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Catalog Number AR002J13
Chemical Name Carbamic acid, N-[(1R,2R)-2-(1,1-dimethylethoxy)-1-(hydroxymethyl)propyl]-, 9H-fluoren-9-ylmethyl ester
CAS Number 189337-28-8
Molecular Formula C23H29NO4
Molecular Weight 383.4807
MDL Number MFCD00235950
SMILES OC[C@H]([C@H](OC(C)(C)C)C)NC(=O)OCC1c2ccccc2-c2c1cccc2 

Fmoc-Thr(tBu)-OL is a versatile compound widely used in chemical synthesis for the efficient and selective protection of threonine residues. As a key building block in peptide chemistry, Fmoc-Thr(tBu)-OL plays a crucial role in the synthesis of complex peptides and proteins.This compound is particularly valued for its ability to protect the hydroxyl group of threonine, allowing for precise control over the stepwise assembly of peptide chains. By incorporating Fmoc-Thr(tBu)-OL into the synthesis process, chemists are able to selectively activate and modify specific threonine residues while safeguarding the overall integrity of the peptide structure.In addition to its protective function, Fmoc-Thr(tBu)-OL also serves as a valuable tool for facilitating purification and characterization of peptides. The Fmoc group enables easy removal post-synthesis through standard deprotection methods, leaving behind the desired threonine residue intact. This simplifies downstream purification steps and ensures high-quality peptide products.Overall, Fmoc-Thr(tBu)-OL is an indispensable reagent in peptide synthesis, enabling precise manipulation of threonine residues and streamlined production of complex peptides with high purity and yield. Its versatility and reliability make it a fundamental component in the toolkit of synthetic chemists working towards the development of novel bioactive molecules and pharmaceuticals.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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