2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID

2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID Suppliers list
Company Name: Shandong Fande Pharmaceutical Technology Co., Ltd.  Gold
Tel: 0531-00000000 15552883993
Email: 3180453864@qq.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com
Company Name: Carbott PharmTech Inc.  
Tel: 0535-6385396
Email: info@carbottpharm.com
Company Name: Wuhan Chemwish Technology Co., Ltd  
Tel: 86-027-67849912
Email: sales@chemwish.com
Company Name: Capot Chemical Co., Ltd  
Tel: +86 (0) 571 85 58 67 18
Email:

2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID manufacturers

2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID Basic information
Product Name:2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID
Synonyms:2-oxo-1,3-dihydroindole-6-carboxylic acid;2-Oxoindoline-6-carboxylic acid in stock Factory;Nidanib Impurity 2: 2-oxy-2,3-dihydro-1H-indole-6-carboxylic acid;RARECHEM AL BO 0984;OXINDOLE-6-CARBOXYLIC ACID;2,3-DIHYDRO-2-OXO-1H-INDOLE-6-CARBOXYLIC ACID;2-Oxindole-6-carboxylic acid;2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID
CAS:334952-09-9
MF:C9H7NO3
MW:177.16
EINECS:
Product Categories:blocks;Carboxes;IndolesOxindoles;pharmacetical;Indoline & Oxindole
Mol File:334952-09-9.mol
2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID Structure
2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID Chemical Properties
Boiling point 438.1±45.0 °C(Predicted)
density 1.433±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka3.94±0.20(Predicted)
AppearanceWhite to off-white Solid
Safety Information
Hazard Codes Xi
Risk Statements 36
Safety Statements 26
HS Code 2933998090
MSDS Information
2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID Usage And Synthesis
Synthesis
Methyl 2-oxoindole-6-carboxylate

14192-26-8

2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID

334952-09-9

General procedure for the synthesis of 2-oxoindoline-6-carboxylic acid from methyl 2-oxoindoline-6-carboxylate: Sodium hydroxide solution (1N, 20 mL) was added to a solution of 2-oxoindoline-6-carboxylic acid methyl ester (2 g, 10.46 mmol, 1.00 equiv) in methanol (20 mL). The reaction mixture was stirred at 80 °C for 2 hours. After completion of the reaction, the mixture was cooled to 30 °C, diluted with 50 mL of water and extracted with dichloromethane (2 x 30 mL). The aqueous phases were combined and the pH was adjusted with aqueous hydrochloric acid (6N) to 2. The precipitated solid was collected by filtration and dried to give the title compound 1.28 g (69% yield) as a brown solid.1H NMR (400 MHz, CDCl3) δ: 12.86 (s, 1H), 10.50 (s, 1H), 7.55 (m, 1H), 7.32-7.30 (m. 2H), 3.56 (s, 2H).

References[1] Patent: US2015/284327, 2015, A1. Location in patent: Paragraph 0215; 0216
[2] Patent: WO2006/64044, 2006, A1. Location in patent: Page/Page column 21-22
2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID Preparation Products And Raw materials
Raw materialsMethyl 2-oxoindole-6-carboxylate-->2,3-Dioxoindoline-6-carboxylic acid-->Sodium hydroxide-->Methanol
Tag:2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID(334952-09-9) Related Product Information
2-OXO-2,3-DIHYDRO-1H-INDOLE-5-CARBOXYLIC ACID METHYL ESTER 2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID METHYL ESTER N-methyl-N-(4-nitrophenyl)-2-(piperazin-1-yl)acetamide Methyl 1-acetyl-2-oxoindoline-6-carboxylate Oxindole 1-Chloro-4-(trimethoxymethyl)benzene 1,3-DiMethyl 2-[4-(Methoxycarbonyl)-2-nitrophenyl]propanedioate Nintedanib Impurity 76 N-methyl-2-(4-methylpiperazin-1-yl)-N-(4-nitrophenyl)acetamide (Z)-methyl 3-(((4-(methylamino)phenyl)amino)(phenyl)methylene)-2-oxoindoline-6-carboxylate N-Methyl-4-nitroaniline Nintedanib Impurity 67 1,2-dichloro-4-(dichloromethyl)benzene BIBF 1202 Nintedanib Impurity 62 Ethanesulfonic acid isopropyl ester 2-Oxo-2,3-dihydro-1H-indole-6-carboxylic acid ethyl ester 2-Propanesulfonic acid sodium salt mon&