TIMTEC-BB SBB002930

TIMTEC-BB SBB002930 - Names and Identifiers

Name	5-fluoroindole-3-carboxaldehyde
Synonyms	AKOS JY2083653 TIMTEC-BB SBB002930 5-Fluoro-3-formylindole 5-FLUOROINDOLE-3-ALDEHYDE 5-FLUOROINDOLE-3-CARBALDEHYDE 5-FLUOROINDOLE-3-CARBOXALDEHYDE 5-fluoroindole-3-carboxaldehyde 5-fluoro-1H-indole-3-carbaldehyde 5-FLUORO-1H-INDOLE-3-CARBALDEHYDE 5-FLUORO-1H-INDOLE-3-CARBOXALDEHYDE
CAS	2338-71-8
InChI	InChI=1/C9H6FNO/c10-7-1-2-9-8(3-7)6(5-12)4-11-9/h1-5,11H

TIMTEC-BB SBB002930 - Physico-chemical Properties

Molecular Formula	C9H6FNO
Molar Mass	163.15
Density	1.385±0.06 g/cm3(Predicted)
Melting Point	164°C
Boling Point	342.4±22.0 °C(Predicted)
Flash Point	160.9°C
Vapor Presure	7.53E-05mmHg at 25°C
Appearance	Solid
Color	yellow to green
BRN	1449216
pKa	14.66±0.30(Predicted)
Storage Condition	Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
Sensitive	Air Sensitive
Refractive Index	1.695
MDL	MFCD00022719

TIMTEC-BB SBB002930 - Risk and Safety

Hazard Symbols	Xi - Irritant
Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing.
WGK Germany	3
HS Code	29339900
Hazard Class	IRRITANT

TIMTEC-BB SBB002930 - Introduction

It is an organic compound with the chemical formula C9H6FNO. It has the appearance of a pale yellow solid.

Regarding the properties of this compound, there are the following points:
1. Melting Point: about 63-66 ℃.
2. Boiling point: About 286-288 ℃.
3. Solubility: It has high solubility in some organic solvents, such as dimethyl sulfoxide and dichloromethane.
4. Chemical reaction: It has an aldehyde functional group and can undergo typical aldehyde reactions, such as electrophilic addition, oxidation, etc.

There is not much research on the use of this compound, but it may be used as an intermediate in organic synthesis to prepare other organic compounds. Because of its structure containing fluorine atoms and indole nuclei, it may have potential applications in anti-tumor and other aspects.

Methods of Preparation:
A common preparation method is to start from the starting material of indole, first react indole with trifluorosuccinyl chloride (TFAA) to obtain trifluorosuccinyl indole (trifluoroacetate indole), the product is then reacted with hydrazine hydrate to remove the trifluoroacetyl group to obtain the calcium halide.

There is no detailed report on the safety information of this compound. Because it is an organic compound, it should generally be handled correctly in the laboratory and comply with relevant laboratory safety practices. The compound may have potential effects on the human body, so appropriate protective measures should be taken when using it, such as wearing protective glasses and gloves, and ensuring a well-ventilated laboratory environment. If it needs to be applied to commercial production or other specific scenarios, relevant safety assessment and control measures should be made according to the specific situation.

Last Update：2024-04-10 22:29:15