CAS 3262-72-4
:BOC-L-serina
Descripción:
BOC-L-serina, también conocido como tert-butiloxicarbonilo-L-serina, es un derivado del aminoácido serina, caracterizado por la presencia de un grupo protector de tert-butiloxicarbonilo (BOC). Este compuesto se utiliza comúnmente en la síntesis de péptidos para proteger el grupo amino de la serina, facilitando la formación de enlaces peptídicos sin interferencia del grupo amino. BOC-L-serina es típicamente un sólido cristalino blanco a blanco sucio, y es soluble en disolventes orgánicos como metanol y dimetilsulfóxido (DMSO), pero menos soluble en agua. El grupo BOC se puede eliminar en condiciones ácidas, permitiendo la regeneración del grupo amino libre para reacciones posteriores. Su estructura molecular incluye un grupo hidroxilo, que contribuye a su reactividad y capacidad para participar en varios procesos bioquímicos. BOC-L-serina se utiliza en aplicaciones de investigación y farmacéuticas, particularmente en la síntesis de péptidos y otros compuestos bioactivos. El manejo y almacenamiento adecuados son esenciales, como con muchas sustancias químicas, para mantener la estabilidad y prevenir la degradación.
Fórmula:C8H15NO5
InChI:InChI=1S/C8H15NO5/c1-8(2,3)14-7(13)9-5(4-10)6(11)12/h5,10H,4H2,1-3H3,(H,9,13)(H,11,12)/t5-/m0/s1
Clave InChI:InChIKey=FHOAKXBXYSJBGX-YFKPBYRVSA-N
SMILES:[C@@H](NC(OC(C)(C)C)=O)(C(O)=O)CO
Sinónimos:- (2S)-2-[(tert-butoxycarbonyl)amino]-3-hydroxypropanoate
- (2S)-2-[[(tert-Butoxy)carbonyl]amino]-3-hydroxypropanoic acid
- (2S)-3-Hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
- (S)-2-(tert-Butoxycarbonylamino)-3-hydroxypropanoic acid
- (S)-2-[(tert-Butoxycarbonyl)amino]-3-hydroxypropionic acid
- <span class="text-smallcaps">L</span>-N-tert-Butoxycarbonylserine
- <span class="text-smallcaps">L</span>-Serine, N-[(1,1-dimethylethoxy)carbonyl]-
- BOC-<span class="text-smallcaps">L</span>-serine
- BOC-Serine
- Boc-L-Ser-OH
- Boc-Ser-OH
- N-(tert-Butoxycarbonyl)-<span class="text-smallcaps">L</span>-serine
- N-(tert-Butoxycarbonyl)-L-serine
- N-(tert-butoxycarbonyl)serine
- N-BOC-<span class="text-smallcaps">L</span>-serine
- N-[(1,1-Dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-serine
- N-t-Butoxycarbonylserine
- N-tert-Butyloxycarbonyl-<span class="text-smallcaps">L</span>-serine
- N-tert-Butyloxycarbonylserine
- NSC 164056
- Serine, N-carboxy-, N-tert-butyl ester, <span class="text-smallcaps">L</span>-
- N-tert-Butyloxycarbonyl-L-serine
- Serine, N-carboxy-, N-tert-butyl ester, L-
- N-[(1,1-Dimethylethoxy)carbonyl]-L-serine
- Ver más sinónimos
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Encontrado 12 productos.
N-(tert-Butoxycarbonyl)-L-serine
CAS:Fórmula:C8H15NO5Pureza:>97.0%(T)(HPLC)Forma y color:White to Almost white powder to crystalPeso molecular:205.21N-Boc-L-serine, 98% (dry wt.), may cont. up to 10% water
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Fórmula:C8H15NO5Pureza:98%Forma y color:White, Powder or crystalline powderPeso molecular:205.21Boc-Ser-OH Bachem Quality Grade
CAS:Educt for the synthesis of Boc-Ser β-lactone, a useful synthon for obtaining stereochemically pure β-substituted α-amino acids. Building block for the incorporation of O-acyl isopeptide bonds during Fmoc-SPPS.Fórmula:C8H15NO5Pureza:> 99%Forma y color:WhitePeso molecular:205.21Serine, N-[(1,1-dimethylethoxy)carbonyl]-
CAS:Fórmula:C8H15NO5Pureza:96%Forma y color:SolidPeso molecular:205.2084L-Serine-2,3,3-d3-N-t-BOC
CAS:Fórmula:HOCD2CD(NHtBOC)COOHPureza:98 atom % DForma y color:White SolidPeso molecular:208.22(2S)-2-[(tert-Butoxycarbonyl)amino]-3-hydroxypropanoic acid
CAS:(2S)-2-[(tert-Butoxycarbonyl)amino]-3-hydroxypropanoic acidFórmula:C8H15NO5Pureza:96%Forma y color: white solidPeso molecular:205.2084g/molBoc-L-serine
CAS:<p>Boc-L-serine is a cyclic peptide that contains a hydroxyl group and a trifluoroacetate group. It has been shown to have anticancer activity in experimental models, but the mechanism of action is not fully understood. Boc-L-serine inhibits the growth of cancer cells by binding to P2Y receptors and blocking the downstream signaling cascade. This drug also has been shown to be stereospecific with respect to its biological activity, which may be due to hydrogenation of nitrogen atoms on the molecule.</p>Fórmula:C8H15NO5Pureza:Min. 95%Forma y color:White PowderPeso molecular:205.21 g/molBoc-Ser-OH
CAS:<p>M03318 - Boc-Ser-OH</p>Fórmula:C8H15NO5Pureza:95%Forma y color:Solid, Crystalline PowderPeso molecular:205.21BOC-L-Serine extrapure, 99%
CAS:Fórmula:C8H15NO5Pureza:min. 99.0%Forma y color:White, Crystalline powderPeso molecular:205.20N-Boc-L-Serine
CAS:Producto controlado<p>Applications N-Boc-L-serine is an N-Boc-protected form of L-Serine (S270975). L-Serine is a nonessential amino acid that is required for the synthesis of sphingolipids and phosphatidylserine, compounds that are important for central nervous system neuronal survival. L-Serine is also important in intermediary metabolism in eukaryotic cells.<br>References de Koning, T., et al.: Biochem. J., 371, 653 (2003); Furuya, S.: Asia Pac. J. Clin. Nutr., 17, 312 (2008); Hirabayashi, Y. & Furuya, S.: Prog. Lipid. Res., 47, 188 (2008)<br></p>Fórmula:C8H15NO5Forma y color:NeatPeso molecular:205.21











