Dayang Chem (Hangzhou) Co., Ltd. is one of the leading manufacturers and suppliers of methyl 2-methyl-3-nitrobenzoate cas 59382-59-1 in China, specialized in providing high quality customized chemicals. Welcome to wholesale bulk methyl 2-methyl-3-nitrobenzoate cas 59382-59-1 made in China here and get pricelist from our factory. Good service and reasonable price are available.
Product Introduction:
Chemical specifications
|
Appearance |
Almost white crystalline powder |
|
Assay |
99.0%Min |
|
Loss on Drying |
0.5%Max |
We are happy to supply the most current specifications and analysis report if needed.
Applications
Methyl 2-methyl-3-nitrobenzoate may be used in the synthesis of methyl indole-4-carboxylate, 5-aminoisoquinolin-1(2H)-one, 5-nitroisocoumarin and [2-(4-fluorophenyl)-1H-indol-4-yl]-1-pyrrolidinylmethanone. It may also be used in the preparation of substituted nitrostyrene benzoic acids, via reaction with aromatic aldehydes in the presence of DBU in DMSO; and 4-(hydroxymethyl)-1-tosylindole, via Batcho-Leimgruber modification of the Reissert indole synthesis.
Additional Information:
Package: 25kg net per drum
Transport Information: Not regulated as a dangerous material.
Documentation: Full compliance package (SDS, COA)
We ship globally via DHL, FedEx, UPS, air freight sea freight, with full customs support and documentation, and specialized packaging for hazardous materials that comply with IATA/IMDG standards. Additionally, we offer real-time tracking and insurance services to ensure safe delivery.


Payment method
Paypal ; Wire Transfer/Telegraphic Transfer; L/C at sight
Spectrum

Related Articles
[1]. The Chemistry of Indoles. XII. A Facile Route to 5-Nitroisocoumarins and Methyl Indole-4-carboxylate. Masanori S, et al.
Chem. Pharm. Bull. 29(1) , 249-53, (1981)
[2]. Preparation of 2-arylindole-4-carboxylic amide derivatives. Kuethe JT and Davies LW.
Tetrahedron 62(49) , 11381-90, (2006)
[3]. Synthesis of 2-Arylindole-4-Carboxylic Amides:[2-(4-Fluorophenyl)-1H-Indol-4-YL]-1-Pyrrolidinylmethanone. Kuethe JT and Beutner GL.
Organic Synth. , 92-104, (2009)
Br. J. Pharmacol. 130 , 843-850, (2000)


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