959581-98-7

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959581-98-7 Structure

Identification	Back Directory
[Name] (2S,4R)-1-(tert-butoxycarbonyl)-4-(prop-2-ynyl)pyrrolidine-2-carboxylic acid
[CAS] 959581-98-7
[Synonyms] Boc-(R)-4-propargyl-L-proline Boc-(R)-γ-propargyl-L-proline Boc-(4R)-4-propargyl-L-proline Boc-(R)-4-(2-propynyl)-L-proline (Tert-Butoxy)Carbonyl (R)-γ-propynyl-L-Pro N-(t-Butoxycarbonyl)-trans-4-propynyl-L-proline (2S,4R)-1-(tert-butoxycarbonyl)-4-(prop-2-ynyl)pyrrolidine-2-carboxylic acid Boc-(2S,4R)-1-(tert-butoxycarbonyl)-4-(prop-2-ynyl)pyrrolidine-2-carboxylicacid (2S,4R)-1-[(tert-butoxy)carbonyl]-4-(prop-2-yn-1-yl)pyrrolidine-2-carboxylic acid (2S,4R)-4-(2-Propyn-1-yl)-1,2-pyrrolidinedicarboxylic acid 1-(1,1-dimethylethyl) ester (2S,4R)-1-[(2-methylpropan-2-yl)oxycarbonyl]-4-prop-2-ynylpyrrolidine-2-carboxylic acid 1,2-Pyrrolidinedicarboxylic acid, 4-(2-propyn-1-yl)-, 1-(1,1-dimethylethyl) ester, (2S,4R)-
[Molecular Formula] C13H19NO4
[MDL Number] MFCD06659253
[MOL File] 959581-98-7.mol
[Molecular Weight] 253.294

Chemical Properties	Back Directory
[Melting point ] 95-97℃
[storage temp. ] 2-8°C
[form ] lumps
[Optical Rotation] [α]/D -34.0±2°, c = 1% in ethanol
[Major Application] peptide synthesis
[InChI] 1S/C13H19NO4/c1-5-6-9-7-10(11(15)16)14(8-9)12(17)18-13(2,3)4/h1,9-10H,6-8H2,2-4H3,(H,15,16)/t9-,10+/m1/s1
[InChIKey] DMBBSZBBZZUEMF-ZJUUUORDSA-N
[SMILES] CC(C)(C)OC(=O)N1C[C@H](CC#C)C[C@H]1C(O)=O

Safety Data	Back Directory
[WGK Germany ] 3
[Storage Class] 13 - Non Combustible Solids

Hazard Information	Back Directory
[Uses] (2S,?4R)?-?1-?(tert-?Butoxycarbonyl)?-?4-?(prop-?2-?yn-?1-?yl)?pyrrolidine-?2-?carboxylic Acid is a chiral reagent used in organic synthesis.
[reaction suitability] reaction type: Boc solid-phase peptide synthesis reaction type: click chemistry

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