141452-01-9

141452-01-9 - Names and Identifiers

Name	methyl indoline-5-carboxylate
Synonyms	methyl indoline-5-carboxylate Methyl indoline-5-carboxylate methyl 2,3-dihydro-1H-indole-5-carboxylate Methyl 2,3-dihydro-1H-indole-5-carboxylate 2,3-Dihydro-1H-indol-5-carboxylic acid methyl ester 1H-Indole-5-carboxylicacid, 2,3-dihydro-, methyl ester 1H-indole-5-carboxylic acid, 2,3-dihydro-, methyl ester
CAS	141452-01-9
InChI	InChI=1/C10H11NO2/c1-13-10(12)8-2-3-9-7(6-8)4-5-11-9/h2-3,6,11H,4-5H2,1H3

141452-01-9 - Physico-chemical Properties

Molecular Formula	C10H11NO2
Molar Mass	177.2
Density	1.162±0.06 g/cm3(Predicted)
Melting Point	67-69 °C
Boling Point	331.0±31.0 °C(Predicted)
Flash Point	153.956°C
Solubility	DMSO (Sparingly), Methanol (Slightly)
Vapor Presure	0mmHg at 25°C
Appearance	Solid
Color	Off-White
pKa	2.65±0.20(Predicted)
Storage Condition	Keep in dark place,Sealed in dry,2-8°C
Refractive Index	1.555

141452-01-9 - Introduction

Indoline-5-carboxylic acid methyl ester, also known as indoline-5-carboxylic acid methyl ester, is an organic compound. The following is an introduction to the properties, uses, preparation methods and safety information of indoline -5-carboxylic acid methyl ester:

Nature:
-Appearance: Indoline -5-methyl formate is a colorless liquid.
-Molecular formula: C12H9NO2
-Molecular weight: 199.21g/mol
-Melting point: No definite melting point data.
-Boiling point: about 250°C (exact boiling point data may vary).
-Solubility: Soluble in organic solvents such as ethanol and dichloromethane, insoluble in water.

Use:
Indoline -5-carboxylic acid methyl ester has many uses in organic synthesis, such:
-As an intermediate in organic synthesis, it can be used to synthesize indoline derivatives and other organic compounds.
-In the pharmaceutical field, it can be used to synthesize anti-cancer drugs, etc.
-It can be used as an intermediate for electronic materials, such as organic light-emitting diodes (OLED).
-For chemical research and organic synthesis reactions in the laboratory.

Preparation Method:
Indoline-5-carboxylic acid methyl ester is usually prepared by the following steps:
1. First, indoline -5-formic acid is reacted with formic anhydride under acidic conditions to generate indoline -5-carboxylic acid methyl ester.
2. After the reaction is completed, the desired product is purified by distillation or other methods.

Safety Information:
As an organic compound, indoline-5-carboxylic acid methyl ester has certain safety risks. Here is the relevant safety information:
-May be irritating to eyes and skin, be careful when touching.
-Avoid contact with strong oxidants during use or storage.
-Wear appropriate personal protective equipment such as goggles, gloves and lab coats when handling or handling.
-should be used in well-ventilated conditions, avoid inhalation of vapor or dust.
-If ingested or inhaled, seek medical help immediately and provide information about the chemical.

It should be noted that for the use and operation of chemicals, please strictly follow the relevant safety operation procedures and use them under the guidance of professionals.

Last Update：2024-04-09 21:01:54