CAS 13139-14-5
:N-tert-Butoxycarbonyl-L-tryptophan
Description:
N-tert-Butoxycarbonyl-L-tryptophan, commonly referred to as Boc-L-tryptophan, is a derivative of the amino acid tryptophan, characterized by the presence of a tert-butoxycarbonyl (Boc) protecting group. This compound is typically used in peptide synthesis as a protecting group for the amino group of tryptophan, which helps to prevent unwanted reactions during the synthesis process. Boc-L-tryptophan is a white to off-white solid that is soluble in organic solvents such as dichloromethane and dimethylformamide, but it is less soluble in water. The presence of the indole side chain in tryptophan contributes to its unique properties, including its ability to absorb ultraviolet light. The compound is stable under acidic conditions but can be deprotected under basic conditions or through the use of specific reagents, allowing for the subsequent formation of peptides. Its applications extend to the fields of biochemistry and pharmaceuticals, particularly in the synthesis of bioactive peptides and proteins.
Formula:C16H20N2O4
InChI:InChI=1S/C16H20N2O4/c1-16(2,3)22-15(21)18-13(14(19)20)8-10-9-17-12-7-5-4-6-11(10)12/h4-7,9,13,17H,8H2,1-3H3,(H,18,21)(H,19,20)/t13-/m0/s1
InChI key:InChIKey=NFVNYBJCJGKVQK-ZDUSSCGKSA-N
SMILES:C([C@H](NC(OC(C)(C)C)=O)C(O)=O)C=1C=2C(NC1)=CC=CC2
Synonyms:- (2S)-2-[(tert-butoxycarbonyl)amino]-3-(1H-indol-3-yl)propanoate
- (2S)-2-[[(tert-Butoxy)carbonyl]amino]-3-(1H-indol-3-yl)propanoic acid
- (2S)-3-(1H-Indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
- (S)-2-(((tert-Butoxy)carbonyl)amino)-3-(1H-indol-3-yl)propanoic acid
- (S)-2-[(tert-Butoxycarbonyl)amino]-3-(1H-indol-3-yl)propionic acid
- <span class="text-smallcaps">L</span>-Tryptophan, N-[(1,1-dimethylethoxy)carbonyl]-
- Boc-L-tryptophan
- Boc-Trp-OH
- N-(tert-Butoxycarbonyl)-<span class="text-smallcaps">L</span>-tryptophan methyl ester
- N-(tert-butoxycarbonyl)-D-tryptophan
- N-(tert-butoxycarbonyl)tryptophan
- N-BOC-<span class="text-smallcaps">L</span>-Trp-OH
- N-Boc-<span class="text-smallcaps">L</span>-tryptophan
- N-[(1,1-Dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-tryptophan
- N-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-tryptophan
- N-tert-Butyloxycarbonyl-<span class="text-smallcaps">L</span>-tryptophan
- N<sup>α</sup>-BOC-<span class="text-smallcaps">L</span>-tryptophan
- N<sup>α</sup>-tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-tryptophan
- N<sup>α</sup>-tert-Butoxycarbonyltryptophan
- NSC 334306
- Tryptophan, N-carboxy-, N-tert-butyl ester
- Tryptophan, N-carboxy-, N-tert-butyl ester, <span class="text-smallcaps">L</span>-
- tert-Butoxycarbonyl-<span class="text-smallcaps">L</span>-tryptophan
- tert-Butyloxycarbonyl-<span class="text-smallcaps">L</span>-tryptophan
- tert-Butoxycarbonyl-L-tryptophan
- Tryptophan, N-carboxy-, N-tert-butyl ester, L-
- N-[(1,1-Dimethylethoxy)carbonyl]-L-tryptophan
- See more synonyms
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Found 7 products.
N-(tert-Butoxycarbonyl)-L-tryptophan
CAS:Formula:C16H20N2O4Purity:>98.0%(HPLC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:304.35Boc-Trp-OH
CAS:M03328 - Boc-Trp-OHFormula:C16H20N2O4Purity:97%Color and Shape:Powder or SolidMolecular weight:304.346Boc-L-Trp-OH
CAS:Boc-L-Trp-OH is a receptor binding molecule that has been shown to have an inhibitory effect on the receptor. The acidic pH of the molecule and its bifunctional nature allow it to bind to the receptor, which is found in the acidic environment of the stomach. This chemical also has an acidic reactive site that can react with hydrogen fluoride. Boc-L-Trp-OH binds to human protein, specifically amino acid residues such as arginine, lysine, and histidine. It also has a reactive site that can be used in chromatographic binding experiments.Formula:C16H20N2O4Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:304.34 g/molBOC-L-Tryptophan extrapure, 99%
CAS:Formula:C16H20N2O4Purity:min. 99%Color and Shape:White to off-white, PowderMolecular weight:304.34






