| Identification | Back 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 Properties | Back 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 Information | Back 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. |
|
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Alfa Aesar
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Energy Chemical
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http://www.energy-chemical.com |
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T&W GROUP
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| Company Name: |
Sigma-Aldrich
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https://www.sigmaaldrich.cn |
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