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About This Item
Empirical Formula (Hill Notation):
C10H11NO
CAS Number:
Molecular Weight:
161.20
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Pricing and availability is not currently available.
Assay
98%
mp
76-79 °C (lit.)
SMILES string
COc1ccc2[nH]ccc2c1C
InChI
1S/C10H11NO/c1-7-8-5-6-11-9(8)3-4-10(7)12-2/h3-6,11H,1-2H3
InChI key
RISMXZVKSIWLMK-UHFFFAOYSA-N
General description
5-Methoxy-4-methylindole or 5-methoxy-4-methyl-1H-indole is a substituted 1H-indole. Its efficacy as a substrate for indigoid production has been evaluated.[1]
Application
- Reactant for preparation of β-carboline-1-carboxylic acids as inhibitors of mitogen activated protein kinase-activated protein kinase 2
- Reactant for preparation of indolyl and isoquinolinyl anthranilates as PPARδ partial agonists
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
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Zhongliu-Liu Wu et al.
Chemistry & biodiversity, 2(1), 51-65 (2006-12-29)
Glycogen synthase kinase-3 (GSK-3) is a potential drug target for a number of human diseases. Some indigoids have been found to be potent inhibitors of GSK-3, and individual compounds with better activity, specificity, and solubility are desired. In this work
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