525898
甲基(1-甲基吲哚基)-3-乙醛酸酯
97%
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关于此项目
经验公式（希尔记法）:
C12H11NO3
化学文摘社编号:
分子量:
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
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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