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About This Item
Empirical Formula (Hill Notation):
C12H11NO3
CAS Number:
Molecular Weight:
217.22
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
mp
96-100 °C (lit.)
SMILES string
COC(=O)C(=O)c1cn(C)c2ccccc12
InChI
1S/C12H11NO3/c1-13-7-9(11(14)12(15)16-2)8-5-3-4-6-10(8)13/h3-7H,1-2H3
InChI key
SBHIWUQNUXJUMN-UHFFFAOYSA-N
General description
Methyl (1-methylindolyl)-3-glyoxylate can be prepared from 1-methylindole.
Application
- Reactant for synthesis of sotrastaurin analogs
- Reactant for preparation of protein kinase C (PKC) inhibitors
- Reactant for preparation of indolyl diols
Methyl (1-methylindolyl)-3-glyoxylate may be used to synthesize 3-[(1-methyl)-3-indolyl]-4-(3-indolyl)-1H-pyrrole-2,5-dione and 3,4-[(1-methyl)-3-indolyl]-1H-pyrrole-2,5-dione.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
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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Find documentation for the products that you have recently purchased in the Document Library.
A New, Efficient Method for the Synthesis of Bisindolylmaleimides.
Margaret M. Faul et al.
The Journal of organic chemistry, 63(17), 6053-6058 (2001-10-24)
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