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5-bromoindole-2-carboxylic acid

5-bromoindole-2-carboxylic acid

CAS: 7254-19-5

Molecular Formula: C9H6BrNO2

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5-bromoindole-2-carboxylic acid - Names and Identifiers

Name 5-bromoindole-2-carboxylic acid
Synonyms AKOS JY2082545
5-Bromo-2-indolecarboxylic acid
5-bromoindole-2-carboxylic acid
5-BROMOINDOLE-2-CARBOXYLIC ACID
5-BROMO-2-INDOLECARBOXYLIC ACID
5-BroMo-1H-indol-2-carboxylic acid
5-BROMO-1H-INDOLE-2-CARBOXYLIC ACID
5-bromo-1H-indole-2-carboxylic acid
1H-INDOLE-2-CARBOXYLIC ACID, 5-BROMO-
5-bromoindole-2-carboxylicacid5-Bromoindole-2-carboxylicacid
CAS 7254-19-5
InChI InChI=1/C9H6BrNO2/c10-6-1-2-7-5(3-6)4-8(11-7)9(12)13/h1-4,11H,(H,12,13)

5-bromoindole-2-carboxylic acid - Physico-chemical Properties

Molecular FormulaC9H6BrNO2
Molar Mass240.05
Density1.838±0.06 g/cm3(Predicted)
Melting Point287-288
Boling Point470.9±25.0 °C(Predicted)
Flash Point238.611°C
Vapor Presure0mmHg at 25°C
AppearanceSolid
ColorWhite to Light yellow to Light orange
pKa4.25±0.30(Predicted)
Storage Condition-20°C
Refractive Index1.749
MDLMFCD00022705

5-bromoindole-2-carboxylic acid - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S37/39 - Wear suitable gloves and eye/face protection
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
WGK Germany3
HS Code29339980
Hazard ClassIRRITANT

5-bromoindole-2-carboxylic acid - Introduction

Acid is an organic compound with the chemical formula C9H6BrNO2.

The following are some properties and characteristics of acid:

Nature:
-Appearance: acid is a white to yellowish crystalline solid.
-Solubility: It is soluble in some organic solvents at room temperature, such as dimethyl sulfoxide and dimethylformamide.

Use:
-acid is a commonly used organic synthesis intermediate, commonly used in the synthesis of drugs, pesticides and dyes and other compounds.

Preparation Method:
-or acid can be prepared by the following steps:
1. Starting from indole, bromination reaction is carried out with bromine gas under alkaline conditions, and bromine is added to the C5 position on the indole ring to obtain 5-bromoindole.
2. then 5-bromo indole and cyanoacetate reaction, nucleophilic addition occurs, generating 5-bromo indole -2-carboxylic acid ethyl ester.
3. Finally, hydrolyze ethyl 5-bromoindole-2-carboxylate to obtain acid.

Safety Information:
-the safety information of acid is limited, but general laboratory safety procedures should be followed when handling and using.
-It may be irritating to the eyes, skin and respiratory tract, so wear appropriate personal protective equipment, such as safety glasses and gloves.
-The storage and handling of oxidizing chemicals should be carried out in accordance with local regulations.
Last Update:2024-04-09 21:00:56
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