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1007882-59-8

1007882-59-8 Structure

1007882-59-8 Structure
IdentificationBack Directory
[Name]

(S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
[CAS]

1007882-59-8
[Synonyms]

EOS-61040
(S)-tert-butyl 2-(4-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
tert-Butyl (S)-2-(4-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
(S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
tert-butyl (S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
tert-butyl (2S)-2-(4-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
tert-butyl (2S)-2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate
(S)-2-(5-bromo-1H-imidazol-2-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester
1-Pyrrolidinecarboxylic acid, 2-(5-bromo-1H-imidazol-2-yl)-, 1,1-dimethylethyl ester, (2S)-
[EINECS(EC#)]

813-157-2
[Molecular Formula]

C12H18BrN3O2
[MDL Number]

MFCD16620748
[MOL File]

1007882-59-8.mol
[Molecular Weight]

316.19
Chemical PropertiesBack Directory
[Boiling point ]

469.3±35.0 °C(Predicted)
[density ]

1.444±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[pka]

11.13±0.10(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C12H18BrN3O2/c1-12(2,3)18-11(17)16-6-4-5-8(16)10-14-7-9(13)15-10/h7-8H,4-6H2,1-3H3,(H,14,15)/t8-/m0/s1
[InChIKey]

GAZHEEFWONCMGH-QMMMGPOBSA-N
[SMILES]

N1(C(OC(C)(C)C)=O)CCC[C@H]1C1NC(Br)=CN=1
Questions And AnswerBack Directory
[Uses]

It can be used as a chemical and pharmaceutical intermediate in the laboratory research and development process.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933299065
Spectrum DetailBack Directory
[Spectrum Detail]

(S)-tert-butyl 2-(5-bromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate(1007882-59-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

To a preparation of (S)-tert-butyl 2-(4,5-dibromo-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (12.5 g, 31.5 mmol) in a mixture of dioxane (400 ml) and H2O (400 ml) was added a solution of Na2SO3 (43.7 g, 347 mmol) in H2O (400 ml) and heated to reflux for 2
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