525898
Methyl (1-methylindolyl)-3-glyoxylate
97%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C12H11NO3
CAS Number:
Molecular Weight:
217.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
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
SMILES string
COC(=O)C(=O)c1cn(C)c2ccccc12
InChI key
SBHIWUQNUXJUMN-UHFFFAOYSA-N
assay
97%
mp
96-100 °C (lit.)
Quality Level
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
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)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service