ChemicalBook--->CAS DataBase List--->959581-98-7

959581-98-7

959581-98-7 Structure

959581-98-7 Structure
IdentificationBack 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 PropertiesBack 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 DataBack Directory
[WGK Germany ]

3
[Storage Class]

13 - Non Combustible Solids
Hazard InformationBack 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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