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1-Methyl-2-oxindole / 5 G

Purity: 97 %
Synonym: Ba 2777; NSC 97219; 1-Methyloxindole; 1-Methyl-2-indolinone; 1-methylindolin-2-one; 1-Methyl-1,3-dihydroindol-2-one
Molecular Formula: C9H9NO
Molecular Weight: 147.17
SKU: MND-44878
CAS Number: 61-70-1
MDL number: MFCD00030253
Form: solid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 5 G  
117.60 EUR



Safety Information


Hazard Statements

H315
H319
H335

Precautionary Statements

P280
P264
P305 + P351 + P338
P261
P271
P302 + P352

Pictograms



Properties

Signal WordWarning
Flash Point (C)Not available
Flash Point (F)Not available
Melting Point85-88 °C (lit.)

 Product Description

1-Methyl-2-oxindole is a chemical compound commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It possesses unique structural properties that make it valuable in organic synthesis processes.

 

Application:

1-Methyl-2-oxindole is employed as a key building block in the production of various pharmaceuticals and agrochemicals, contributing to the synthesis of diverse compounds in these industries.

 

 

Articles:

- Aromatic and heteroaromatic annelation studies on 3-[bis(methylthio)methylene]-1-methyloxindole: synthesis of carbazoles and an efficient route to pyrido[2,3-b]indoles

Publication Date: Available online 15 January 2001

J.R Suresh, U.K Syam Kumar, H Ila, H Junjappa

https://doi.org/10.1016/S0040-4020(00)01054-1

 

- Quercetin and 1-methyl-2-oxindole mimic root signaling that promotes spore germination and mycelial growth of Gigaspora margarita

Publication Date: 22 February 2022

Alberto Campos-López, Jaime A. Uribe-López, Verna Cázares-Ordoñez, Roberto Garibay-Orijel, Norma A. Valdez-Cruz & Mauricio A. Trujillo-Roldán

https://doi.org/10.1007/s00572-022-01074-5

 

- An efficient one-pot synthesis of spiro dihydrofuran oxindole and spiro 2-hydroxytetrahydrofuran oxindole derivatives via (3+2) oxidative cycloaddition mediated by CAN

Publication Date: Available online 15 February 2007

G. Savitha, S.K. Niveditha, D. Muralidharan, P.T. Perumal

https://doi.org/10.1016/j.tetlet.2007.02.045