CAS 37784-17-1
:N-Boc-D-proline
- (2R)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylate
- 1-Boc-D-proline
- Boc-D-Pro-OH
- Boc-D-proline
N-(tert-Butoxycarbonyl)-D-proline
CAS:Formula:C10H17NO4Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:215.25N-Boc-D-proline, 98+%
CAS: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
Formula:C10H17NO4Purity:98+%Color and Shape:White, Crystals or powder or crystalline powderMolecular weight:215.25Boc-D-Pro-OH
CAS:Bachem ID: 4000664.
Formula:C10H17NO4Purity:> 99.5%Color and Shape:WhiteMolecular weight:215.25Ref: IN-DA0035CW
5g20.00€10g25.00€1kg190.00€25g29.00€50g35.00€5kgTo inquire100g56.00€10kgTo inquire500g135.00€N-Boc-D-proline
CAS:N-Boc-D-prolinePurity:98%Color and Shape:White PowderMolecular weight:215.25g/molN-Boc-D-proline
CAS:Formula:C10H17NO4Purity:≥ 98.0%Color and Shape:White powder or crystalsMolecular weight:215.25Boc-D-Pro-OH
CAS:M03316 - Boc-D-Pro-OH
Formula:C10H17NO4Purity:97%Color and Shape:Solid, Crystalline Powder or PowderMolecular weight:215.249tert-Butoxycarbonyl-D-proline
CAS:Controlled ProductApplications 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.
References Jung, M., et al.: Bioorg. Med. Chem. Lett., 7, 1655 (1997); Lee, D., et al.: J. Med. Chem,, 44, 2015 (2001)Formula:C10H17NO4Color and Shape:NeatMolecular weight:215.25N-Boc-D-proline
CAS: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%.
Formula:C10H17NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:215.25 g/molBoc-D-Pro-OH
CAS: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.
Formula:C10H17NO4Purity:Min. 95%Molecular weight:215.25 g/molBOC-D-Proline extrapure, 99%
CAS:Formula:C10H17NO4Purity:min. 99%Color and Shape:White, Crystalline compoundMolecular weight:215.30










