≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product Describtion:
tert -Butyl indoline-1-carboxylate is an N-substituted indoline derivative.
Product Application:
Reactant in preparation of aryl alkyl amines via alkylation reactions catalyzed by Pd
Reactant in preparation of allyl- and arylindolines
Reactant in modular indole synthesis of the highly strained CDEF parent tetracycle of nodulisporic acids A and B
Reactant in asymmetric synthesis of β-amino esters via rhodium prolinate complex-catalyzed α-C-H activation / carbenoid insertion reactions
Reactant in preparation of substituted indolines and tetrahydroquinolines via cycloaddition approach
| Pubchem Sid | 488194500 |
|---|---|
| Canonical Smiles | CC(C)(C)OC(=O)N1CCC2=CC=CC=C21 |
| IUPAC Name | tert-butyl 2,3-dihydroindole-1-carboxylate |
| InChIKey | GWAXLDLPPZPQLO-UHFFFAOYSA-N |
| INCHI | 1S/C13H17NO2/c1-13(2,3)16-12(15)14-9-8-10-6-4-5-7-11(10)14/h4-7H,8-9H2,1-3H3 |
| Isomeric SMILES | CC(C)(C)OC(=O)N1CCC2=CC=CC=C21 |
| WGK Germany | 3 |
| PubChem CID | 3663954 |
| Molecular Weight | 219.28 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Indoles and derivatives |
| Subclass | Indolecarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Indolecarboxylic acids |
| Alternative Parents | Benzenoids Carbamate esters Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Indolecarboxylic acid - Benzenoid - Carbamic acid ester - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as indolecarboxylic acids. These are compounds containing a carboxylic acid group linked to an indole. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 D23081028 | Certificate of Analysis | Jan 20, 2026 | T341572 |
| D23081029 | Certificate of Analysis | Jan 20, 2026 | T341572 |
| D23081030 | Certificate of Analysis | Jan 20, 2026 | T341572 |
| D23081031 | Certificate of Analysis | Jan 20, 2026 | T341572 |
| D23081032 | Certificate of Analysis | Jan 20, 2026 | T341572 |
| D23081034 | Certificate of Analysis | Jan 20, 2026 | T341572 |
| Flash Point(°F) | 230 °F |
|---|---|
| Flash Point(°C) | 110 °C |
| Boil Point(°C) | 83-84 °C/0.1 mmHg (lit.) |
| Melt Point(°C) | 46-50 °C (lit.) |
| Molecular Weight | 219.280 g/mol |
| XLogP3 | 2.700 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 219.126 Da |
| Monoisotopic Mass | 219.126 Da |
| Topological Polar Surface Area | 29.500 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 270.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
