ChemicalBook--->CAS DataBase List--->143262-10-6

143262-10-6

143262-10-6 Structure

143262-10-6 Structure
IdentificationBack Directory
[Name]

1-BOC-INDOLINE
[CAS]

143262-10-6
[Synonyms]

1-BOC-INDOLINE
BUTTPARK 52\06-71
1-(tert-Butoxycarbonyl)indoline
TERT-BUTYL INDOLINE-1-CARBOXYLATE
N-(tert-Butoxycarbonyl)-2,3-dihydroindole
tert-butyl 2,3-dihydroindole-1-carboxylate
2,3-dihydroindole-1-carboxylic acid tert-butyl ester
1H-Indole-1-carboxylic acid, 2,3-dihydro-, 1,1-diMethylethyl ester
[Molecular Formula]

C13H17NO2
[MDL Number]

MFCD01318399
[MOL File]

143262-10-6.mol
[Molecular Weight]

219.28
Chemical PropertiesBack Directory
[Melting point ]

46-50 °C(lit.)
[Boiling point ]

83-84 °C0.1 mm Hg(lit.)
[density ]

1.114±0.06 g/cm3(Predicted)
[Fp ]

>230 °F
[pka]

0.84±0.20(Predicted)
[BRN ]

5336249
[CAS DataBase Reference]

143262-10-6
Hazard InformationBack Directory
[Uses]

Reactant in preparation of aryl alkyl amines via alkylation reactions catalyzed by Pd 1 Reactant in preparation of allyl- and arylindolines 2 Reactant in modular indole synthesis of the highly strained CDEF parent tetracycle of nodulisporic acids A and B 3 Reactant in asymmetric synthesis of β-amino esters via rhodium prolinate complex-catalyzed α-C-H activation / carbenoid insertion reactions 4 Reactant in preparation of substituted indolines and tetrahydroquinolines via cycloaddition approach.
[General Description]

tert -Butyl indoline-1-carboxylate is an N-substituted indoline derivative.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
Spectrum DetailBack Directory
[Spectrum Detail]

1-BOC-INDOLINE(143262-10-6)IR
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