CAS 37784-17-1
:N-Boc-D-Prolin
Beschreibung:
N-Boc-D-Prolin, mit der CAS-Nummer 37784-17-1, ist ein Derivat der Aminosäure Prolin, das durch das Vorhandensein einer tert-butyloxycarbonyl (Boc) Schutzgruppe am Stickstoffatom gekennzeichnet ist. Diese Modifikation verbessert seine Stabilität und Löslichkeit, was es zu einem wertvollen Zwischenprodukt in der Peptidsynthese und der organischen Chemie macht. N-Boc-D-Prolin ist typischerweise ein weißes bis off-white kristallines Feststoff und ist in gängigen organischen Lösungsmitteln wie Dichlormethan und Dimethylformamid löslich, aber weniger löslich in Wasser. Die Boc-Gruppe dient als schützende Einheit, die unter sauren Bedingungen entfernt werden kann, was die selektive Deprotektion der Aminogruppe bei Bedarf ermöglicht. Diese Verbindung wird häufig in der Synthese von Peptiden und anderen bioaktiven Molekülen verwendet, da sie die Bildung von Peptidbindungen erleichtert und gleichzeitig die Chiralität des D-Prolin-Restes bewahrt. Ihre strukturellen Merkmale und Reaktivität machen sie zu einem wichtigen Baustein in der medizinischen Chemie und der Arzneimittelentwicklung.
Formel:C10H16NO4
InChl:InChI=1/C10H17NO4/c1-10(2,3)15-9(14)11-6-4-5-7(11)8(12)13/h7H,4-6H2,1-3H3,(H,12,13)/p-1/t7-/m1/s1
SMILES:CC(C)(C)OC(=O)N1CCC[C@@H]1C(=O)[O-]
Synonyme:- (2R)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylate
- 1-Boc-D-proline
- Boc-D-Pro-OH
- Boc-D-proline
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12 Produkte.
N-(tert-Butoxycarbonyl)-D-proline
CAS:Formel:C10H17NO4Reinheit:>98.0%(T)(HPLC)Farbe und Form:White to Almost white powder to crystalMolekulargewicht:215.25N-Boc-D-proline, 98+%
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>Formel:C10H17NO4Reinheit:98+%Farbe und Form:White, Crystals or powder or crystalline powderMolekulargewicht:215.25Boc-D-Pro-OH
CAS:<p>Bachem ID: 4000664.</p>Formel:C10H17NO4Reinheit:> 99.5%Farbe und Form:WhiteMolekulargewicht:215.25Ref: IN-DA0035CW
5g20,00€10g25,00€1kg190,00€25g29,00€50g35,00€5kgNachfragen100g56,00€10kgNachfragen500g135,00€N-Boc-D-proline
CAS:N-Boc-D-prolineReinheit:98%Farbe und Form:White PowderMolekulargewicht:215.25g/molN-Boc-D-proline
CAS:Formel:C10H17NO4Reinheit:≥ 98.0%Farbe und Form:White powder or crystalsMolekulargewicht:215.25Boc-D-Pro-OH
CAS:<p>M03316 - Boc-D-Pro-OH</p>Formel:C10H17NO4Reinheit:97%Farbe und Form:Solid, Crystalline Powder or PowderMolekulargewicht:215.249tert-Butoxycarbonyl-D-proline
CAS:Kontrolliertes Produkt<p>Applications tert-Butoxycarbonyl-D-proline is Boc protected D-proline (P755990). It is used to prepare trichostatin A and trapoxin B analogs as histone deacetylase inhibitors. It is also used to prepare potent and selective nonpeptide inhibitors of caspases 3 and 7.<br>References Jung, M., et al.: Bioorg. Med. Chem. Lett., 7, 1655 (1997); Lee, D., et al.: J. Med. Chem,, 44, 2015 (2001)<br></p>Formel:C10H17NO4Farbe und Form:NeatMolekulargewicht:215.25N-Boc-D-proline
CAS:<p>N-Boc-D-proline is a lipase inhibitor that is used in the preparation of quinine, aldehyde, and carboxylate. N-Boc-D-proline has been shown to inhibit the activity of the sodium channels, which may be due to its ability to bind to the termini of these channels. The inhibition of sodium channels can lead to a decrease in nerve excitability and seizures. N-Boc-D-proline was synthesized by an organocatalytic method using sodium bicarbonate as the catalyst. It was found that this compound was stereoselective with respect to its activity on different enantiomers of chiral substrates. Preparative methods for N-Boc-D-proline include column chromatography or crystallization with diethyl ether or ethyl acetate. The isolated yield is about 99%.</p>Formel:C10H17NO4Reinheit:Min. 95%Farbe und Form:PowderMolekulargewicht:215.25 g/molBoc-D-Pro-OH
CAS:<p>Boc-D-Pro-OH is a model compound for the synthesis of peptides. Boc-D-Pro-OH has been used in many surface-enhanced Raman spectroscopy studies to investigate the stereochemistry of glycosidic bonds. It has also been used in pharmacokinetic studies to investigate the drug's absorption, distribution, metabolism, and excretion (ADME) properties. The solute is soluble in water due to its hydrophilic nature. Boc-D-Pro-OH is an enantiomer of Boc-L-Pro-OH and a functional group that contains a trifluoromethyl group. This chemical can be used in Tools for Peptide Synthesis with other compounds to form peptides with specific amino acid sequences.</p>Formel:C10H17NO4Reinheit:Min. 95%Molekulargewicht:215.25 g/molBOC-D-Proline extrapure, 99%
CAS:Formel:C10H17NO4Reinheit:min. 99%Farbe und Form:White, Crystalline compoundMolekulargewicht:215.30










