Skip to Content
Merck
All Photos(1)

Documents

466921

Sigma-Aldrich

1-Methyl-2-oxindole

97%

Synonym(s):

1-Methyl-1,3-dihydroindol-2-one, 1-Methyl-2-indolinone, 1-Methyloxindole, Ba 2777, NSC 97219

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C9H9NO
CAS Number:
Molecular Weight:
147.17
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

solid

mp

85-88 °C (lit.)

SMILES string

CN1C(=O)Cc2ccccc12

InChI

1S/C9H9NO/c1-10-8-5-3-2-4-7(8)6-9(10)11/h2-5H,6H2,1H3

InChI key

RSQUAQMIGSMNNE-UHFFFAOYSA-N

Application

Reactant for preparation of:
  • Fluorescent analogues of strigolactones as affectors of parasitic weed germination and fungal branching
  • Irreversible Nek2 Kinase Inhibitors
  • Anticancer agents
  • Antimalarial agents
  • Antitimor agents
  • Germination stimulants in plants
  • Inducers of NAD(P)H-quinone oxidoreductase 1 (NQO1)
  • Retinoic acid analogs
  • Potential anti-multiple sclerosis agents
  • Inhibitors of human immunodeficiency virus type 1 (HIV-1) integrase

Pictograms

Exclamation mark

Signal Word

Warning

Hazard 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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

An Expedient Stereoselective Synthesis of Spirocyclopropyl Oxindoles from Indolin-2-One/N-Protected Indolin-2-Ones and Bromonitroalkenes.
Roy S and Chen K.
J. Chin. Chem. Soc., 60(6), 597-604 (2013)

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