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Assay
96%
form
solid
mp
120-124 °C
SMILES string
CCOC(=O)c1c[nH]c2ccccc12
InChI
1S/C11H11NO2/c1-2-14-11(13)9-7-12-10-6-4-3-5-8(9)10/h3-7,12H,2H2,1H3
InChI key
XOUHVMVYFOXTMN-UHFFFAOYSA-N
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Application
Reactant for preparation of:
- Indole-based heterocycles for synthesis of indole-based p38 inhibitors and gramines
- Glycine receptor ligands
- Inhibitors of Human 5-Lipoxygenase
- Antimicrobial agents
Precursor to 1,2-aziridinopyrrolo-indoles.
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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The Journal of organic chemistry, 69(6), 1794-1799 (2004-04-03)
A convergent synthetic route to the 1,2-aziridinopyrrolo(1,2-a)indole 34 has been developed. Key features of this route include the deuterium kinetic isotope effect to block undesired indole lithiation during tin-lithium exchange from 27a to 30a, the intramolecular Michael addition to generate
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