5-BROMOTHIOPHENE-2-CARBONITRILE

5-BROMOTHIOPHENE-2-CARBONITRILE - Names and Identifiers

Name	5-bromothiophene-2-carbonitrile
Synonyms	K0431 2-Bromo-5-cyanothiophene 2-Cyano-5-bromothiophene 5-BroMothiophene-2-carbon... 5-Bromo-2-Thiophenecarbonitrile 5-bromothiophene-2-carbonitrile 5-BROMOTHIOPHENE-2-CARBONITRILE 5-Brono-thiophene-2-carbonitrile 2-Thiophenecarbonitrile,5-broMo- 2-thiophenecarbonitrile, 5-bromo-
CAS	2160-62-5
InChI	InChI=1/C5H2BrNS/c6-5-2-1-4(3-7)8-5/h1-2H
InChIKey	YVVHCBNJWHPMCQ-UHFFFAOYSA-N

5-BROMOTHIOPHENE-2-CARBONITRILE - Physico-chemical Properties

Molecular Formula	C5H2BrNS
Molar Mass	188.05
Density	1.694 g/mL at 25 °C (lit.)
Boling Point	124°C/34mmHg(lit.)
Flash Point	214°F
Vapor Presure	0.0829mmHg at 25°C
Specific Gravity	1.619
Maximum wavelength(λmax)	276nm(Benzene)(lit.)
Storage Condition	Keep in dark place,Sealed in dry,Room Temperature
Refractive Index	n20/D 1.6190(lit.)

5-BROMOTHIOPHENE-2-CARBONITRILE - Risk and Safety

Hazard Symbols	Xn - Harmful
Risk Codes	R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R36/37/38 - 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. S36/37 - Wear suitable protective clothing and gloves.
UN IDs	3267
WGK Germany	3
HS Code	29309090

5-BROMOTHIOPHENE-2-CARBONITRILE - Introduction

It is an organic compound with the chemical formula C6H3BrNS. The following is a description of its nature, use, preparation and safety information:

Nature:
-Appearance: Colorless to light yellow crystal
-Solubility: Soluble in organic solvents such as ethanol and dichloromethane, insoluble in water
-Melting Point: 62-66 ℃
-Boiling Point: 269-273 ℃
-Molecular weight: 195.06g/mol

Use:
It is an important organic synthesis intermediate compound, which is widely used in the fields of pharmacy, pesticide, dye and photovoltaic. It can be used in the synthesis of other organic compounds, used to construct the skeleton structure of thiophene compounds, so as to obtain the target compounds with specific functions.

Method:
Synthesis can be carried out by the following steps:
1. Under alkaline conditions, thiophene reacts with bromoacetonitrile to generate pyridine.
2. After appropriate purification and crystallization steps, the pure product is obtained.

Safety Information:
-may cause irritation to the eyes, skin and respiratory system, so wear personal protective equipment such as protective gloves, glasses and masks during operation.
-Avoid inhaling its dust or contact with skin.
-In case of accidental use or contact, seek medical attention immediately and provide relevant safety information to the doctor.

Please note that when using and handling chemicals, you must follow safe operating procedures and ensure that you operate under appropriate laboratory conditions.

Last Update：2024-04-10 22:29:15