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201940-08-1

201940-08-1 Structure

201940-08-1 Structure
IdentificationBack Directory
[Name]

TERT-BUTYL 5-BROMOISOINDOLINE-2-CARBOXYLATE
[CAS]

201940-08-1
[Synonyms]

N-Boc-5-broMoisoindoline
2-Boc-5-bromo-isoindoline
3-N-Boc-5-Bromoisoindoline
TERT-BUTYL 5-BROMOISOINDOLINE-2-CARBOXYLATE
TERT-BUTYL 5-BROMO-1,3-DIHYDRO-ISOINDOLE-2-CARBOXYLATE
tert-butyl 5-broMo-1,3-dihydro-2H-isoindole-2-carboxylate
tert-butyl 5-broMo-2,3-dihydro-1H-isoindole-2-carboxylate
5-broMo-1,3-dihydroisoindole-2-carboxylic acid tert-butyl ester
5-Bromo-1,3-dihydro-2H-isoindol-2-carboxylic acid tert-butyl ester
2H-Isoindole-2-carboxylic acid, 5-bromo-1,3-dihydro-, 1,1-dimethylethyl ester
[EINECS(EC#)]

819-411-9
[Molecular Formula]

C13H16BrNO2
[MDL Number]

MFCD09953049
[MOL File]

201940-08-1.mol
[Molecular Weight]

298.19
Chemical PropertiesBack Directory
[Boiling point ]

354.7±42.0 °C(Predicted)
[density ]

1.400
[storage temp. ]

Sealed in dry,2-8°C
[pka]

-1.66±0.20(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P260-P280-P271
[HS Code ]

29339900
Hazard InformationBack Directory
[Uses]

tert-Butyl 5-Bromoisoindoline-2-carboxylate is an intermediate used in the synthesis of Isothiazoloquinolones with Enhanced Antistaphylococcal Activities against Multidrug-Resistant Strains. It is also used to prepare substituted isoindolines as inhibitors of dipeptidyl peptidase 8/9 (DPP8/9).
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