N-Boc-L-prolinol

CAS: 69610-40-8

Ref. 3D-FB28954

Produktinformation

• Name: N-Boc-L-prolinol
• Synonyme: Boc-Pro-ol(S)-tert-Butyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate, 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, (S)-2-Hydroxymethyl-Pyrrolidine-1-Carboxylic Acid Tert-Butyl Ester
• CAS: 69610-40-8

Beschreibung

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.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 201.26 g/mol
• Formel: C₁₀H₁₉NO₃
• Reinheit: Min. 95%
• Farbe/Form: White Powder
• InChl: InChI=1S/C10H19NO3/c1-10(2,3)14-9(13)11-6-4-5-8(11)7-12/h8,12H,4-7H2,1-3H3/t8-/m0/s1
• InChI Key: InChIKey=BFFLLBPMZCIGRM-QMMMGPOBSA-N
• SMILES: CC(C)(C)OC(=O)N1CCC[C@H]1CO