Indole-3-acetic Acid Methyl Ester α-OxiMe

Indole-3-acetic Acid Methyl Ester α-OxiMe - Names and Identifiers

Name	HYDROXYIMINO-(1H-INDOL-3-YL)-ACETIC ACID METHYL ESTER
Synonyms	Indole-3-acetic Acid Methyl Ester α-OxiMe Methyl hydroxyiMino-(1H-indole-3-yl)acetate Methyl (2Z)-(hydroxyimino)(1H-indol-3-yl)acetate methyl (2Z)-(hydroxyimino)(1H-indol-3-yl)ethanoate Methyl 2-(N-hydroxyiMino)-2-(1H-indol-3-yl)acetate α-(Hydroxyimino)-1H-indole-3-acetic Acid Methyl Ester HYDROXYIMINO-(1H-INDOL-3-YL)-ACETIC ACID METHYL ESTER Α-(HYDROXYIMINO)-1H-INDOLE-3-ACETIC ACID METHYL ESTER Hydroxyimino-(1H-indole-3-yl)-acetic acid methyl ester 1H-Indole-3-acetic acid, α-(hydroxyimino)-, methyl ester alpha-(Hydroxyimino)-1H-indole-3-acetic acid methyl ester 1H-Indole-3-acetic acid, .alpha.-(hydroxyimino)-, methyl ester 1H-Indole-3-acetic acid, alpha-(hydroxyimino)-, methyl ester, (alphaZ)-
CAS	113975-75-0
InChI	InChI=1/C11H10N2O3/c1-16-11(14)10(13-15)8-6-12-9-5-3-2-4-7(8)9/h2-6,12,15H,1H3/b13-10-

Indole-3-acetic Acid Methyl Ester α-OxiMe - Physico-chemical Properties

Molecular Formula	C11H10N2O3
Molar Mass	218.21
Density	1.345g/cm³
Boling Point	445.871°C at 760 mmHg
Flash Point	223.455°C
Solubility	Ether
Vapor Presure	0mmHg at 25°C
Storage Condition	2-8°C
Refractive Index	1.622

Indole-3-acetic Acid Methyl Ester α-OxiMe - Introduction

Nature:
Hydroxyimino-(1H-indol-3-yl)-acetic acid methyl ester is a white or off-white crystalline solid with a faint aromatic odor. It is soluble in common organic solvents such as ethanol, acetone and chloroform.

Use:
Hydroxyimino-(1H-indol-3-yl)-acetic acid methyl ester is commonly used as an important intermediate in organic synthesis. It can be used to synthesize a variety of drugs, pesticides and dyes and other compounds. In addition, it can also be used in biological research, for example as a substrate for enzyme-catalyzed reactions.

Method:
Synthesis of hydroxyimino-(1H-indol-3-yl)-acetic acid methyl ester can generally be carried out by the following steps: First, indole and methyl formate are esterified to obtain 3-methylformate indole. The 3-carboxylic acid methyl ester indole is then reacted with hydroxylamine to form hydroxyimino-(1H-indol-3-yl)-acetic acid methyl ester.

Safety Information:
Hydroxyimino-(1H-indol-3-yl)-acetic acid methyl ester needs to be safe during use. It is a chemical, please follow the relevant safety procedures. Contact with the skin may cause irritation, should avoid direct contact with the skin. When performing chemical experiments or preparations, you should operate under well-ventilated conditions and wear suitable protective equipment, such as gloves and goggles. If ingested or inhaled by mistake, seek medical attention immediately.

Last Update：2024-04-09 21:01:54