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Product Name: | Fmoc-L-Thr(tBu)-OL | CAS No: | 189337-28-8 |
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M.W: | 383.48 | MF: | C23H29NO4 |
Appearance: | White Powder | Purity: | 98+ |
EINECS No: | - | Storage: | 5-25°C |
Product Description
White Powder Fmoc-L-Thr(tBu)-OL CAS NO. 189337-28-8 Purity 98+
Name: Fmoc-L-Thr(tBu)-OL
CAS NO: 189337-28-8
M.W: 383.48
Appearance: White Powder
Purity: 98+
Synonyms: N-FMOC-L-THR(TBU)-OL;N-FMOC-L-THR(TBU)-OL-N-FMOC-(2R,3R)-2-AMINO-3-T-BUTOXY-1-BUTANOL;N-FMOC-(2R,3R)-2-AMINO-3-T-BUTOXY-1-BUTANOL;N-ALPHA-FMOC-O-T-BUTYL-L-THREONINOL;(9H-fluoren-9-yl)methylN-[(2R,3R)-3-(tert-butoxy)-1-hydroxybutan-2-yl]carbamate;Fmoc-Thr(OtBu)-Ol;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-O-TERT-BUTYL-L-THREONINOL;N-(9-FLUORENYLMETHOXYCARBONYL)-O-T-BUTYL-L-THREONINOL
Application
Peptide Synthesis: FMOC-THR(TBU)-OL is widely used as a building block in solid-phase peptide synthesis. Due to the presence of the Fmoc (9-fluorenylmethoxycarbonyl) protecting group, it can undergo coupling reactions with other amino acids or peptide fragments to progressively build peptide chains of the desired sequence. This compound is particularly useful for synthesizing peptide chains with specific amino acid sequences that are relevant in drug discovery, bioactivity studies, and biochemical research.
Organic Synthesis: Besides peptide synthesis, FMOC-THR(TBU)-OL also finds application as an intermediate in organic synthesis. The functional groups in its structure, such as amino and hydroxyl groups, allow for various chemical transformations, including esterification, amidation, reduction, and others. These reactions can be used to synthesize other complex organic molecules, further expanding its applications in areas like medicinal chemistry and materials science.
Package
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