CAS 69610-40-8
:N-ALPHA-tert-Butoxycarbonyl-L-prolinol
Description:
N-Alpha-tert-Butoxycarbonyl-L-prolinol, with the CAS number 69610-40-8, is an organic compound commonly used in peptide synthesis and as a protecting group in organic chemistry. This compound features a prolinol backbone, which is an amino alcohol derived from proline, and is modified with a tert-butoxycarbonyl (Boc) group. The Boc group serves as a protective moiety for the amino function, allowing for selective reactions without interfering with the amine's reactivity. N-Alpha-tert-Butoxycarbonyl-L-prolinol is typically a white to off-white solid and is soluble in common organic solvents such as dichloromethane and methanol. Its stability under various conditions makes it a valuable intermediate in the synthesis of pharmaceuticals and biologically active compounds. Additionally, the presence of the prolinol structure imparts unique stereochemical properties, which can influence the conformation and biological activity of the resulting peptides. Proper handling and storage are essential, as with many organic compounds, to maintain its integrity and effectiveness in synthetic applications.
Formula:C10H19NO3
InChI:InChI=1/C10H19NO3/c1-10(2,3)14-9(13)11-6-4-5-8(11)7-12/h8,12H,4-7H2,1-3H3/t8-/m1/s1
SMILES:CC(C)(C)OC(=O)N1CCC[C@@H]1CO
Synonyms:- BOC-L-Prolinol
- N-Boc-L-prolinol
- Boc-Pro-ol
- N-(tert-Butoxycarbonyl)-L-prolinol
- (S)-(-)-1-tert-Butoxycarbonyl-2-pyrrolidinemethanol
- Tert-Butyl 2-(Hydroxymethyl)Pyrrolidine-1-Carboxylate
- tert-butyl (2S)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
- tert-butyl (2R)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
- (S)-(-)-1-Boc-2-Pyrrolidinemethanol
- 1-Pyrrolidinecarboxylic acid, 2-(hydroxymethyl)-, 1,1-dimethylethyl ester, (2S)-
- 2-Hydroxymethylpyrrolidine-1-carboxylic acid tert butyl ester
- See more synonyms
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Found 8 products.
N-(tert-Butoxycarbonyl)-L-prolinol
CAS:Formula:C10H19NO3Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:201.27N-Boc-L-prolinol, 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>Formula:C10H19NO3Purity:98+%Color and Shape:crystalline powder, WhiteMolecular weight:201.27tert-Butyl (S)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
CAS:Formula:C10H19NO3Purity:97%Color and Shape:SolidMolecular weight:201.2628Ref: IN-DA0035D1
1g21.00€5g21.00€10g25.00€25g28.00€5kgTo inquire100g52.00€250g100.00€25kgTo inquire500g156.00€50kgTo inquire(2S)-(+)-2-(Hydroxymethyl)pyrrolidine, N-BOC protected
CAS:<p>(2S)-(+)-2-(Hydroxymethyl)pyrrolidine, N-BOC protected</p>Formula:C10H19NO3Purity:≥95%Color and Shape: slightly yellow powderMolecular weight:201.26g/molN-Boc-L-prolinol
CAS:<p>N-Boc-L-prolinol is a chiral proline derivative that has been modified with an allyl group. It is a potent nicotinic acetylcholine antagonist, and it has been shown to have immune functions in vitro. The synthesis of N-Boc-L-prolinol occurs through a three-step process involving the use of organocatalysts, asymmetric synthesis, and stereoselective reactions. This molecule is also useful for the study of apoptotic signaling pathways in cells.</p>Formula:C10H19NO3Purity:Min. 95%Color and Shape:White PowderMolecular weight:201.26 g/moltert-Butyl (S)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
CAS:Controlled Product<p>Applications tert-Butyl (S)-2-(hydroxymethyl)pyrrolidine-1-carboxylate, is a building block used foe the synthesis of novel nicotinic acetylcholine receptor ligands with cognition-enhancing properties. It can also be used in the synthesis of chiral β-amino sulfides and β-amino thiols.<br>References Elliiot, R. L., et al.: Bioorg. Med. Chem. Lett., 6, 2283 (1996); Abreo, M. A., et al.: J. Med. Chem., 39(4), 817 (1996);<br></p>Formula:C10H19NO3Color and Shape:NeatMolecular weight:201.26







