CAS 91895-30-6

2,3-Dichloro-6,7-difluoroquinoxaline

Description:

2,3-Dichloro-6,7-difluoroquinoxaline is a heterocyclic compound characterized by its quinoxaline backbone, which consists of a fused bicyclic structure containing two nitrogen atoms. This compound features two chlorine atoms at the 2 and 3 positions and two fluorine atoms at the 6 and 7 positions of the quinoxaline ring, contributing to its unique chemical properties. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of halogen substituents can influence its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, compounds like 2,3-Dichloro-6,7-difluoroquinoxaline may possess biological activity, making them of interest in pharmaceutical research. Its molecular structure can lead to interesting electronic properties, which may be exploited in materials science and organic electronics. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.

Formula: C₈H₂Cl₂F₂N₂

InChI: InChI=1S/C8H2Cl2F2N2/c9-7-8(10)14-6-2-4(12)3(11)1-5(6)13-7/h1-2H

InChI key: InChIKey=CMQLMJCICYOHDE-UHFFFAOYSA-N

SMILES: FC1=CC2=C(N=C(Cl)C(Cl)=N2)C=C1F

Synonyms:

• 2,3-Dichloro-6,7-difluoroquinoxaline
• 6,7-Difluoro-2,3-dichloroquinoxaline
• Quinoxaline, 2,3-dichloro-6,7-difluoro-

Quinoxaline, 2,3-dichloro-6,7-difluoro-

CAS: 91895-30-6

Formula: C₈H₂Cl₂F₂N₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 235.0177

Ref: IN-DA00IGXK

2,3-Dichloro-6,7-difluoroquinoxaline

CAS: 91895-30-6

2,3-Dichloro-6,7-difluoroquinoxaline

Purity: 97%

Molecular weight: 235.02g/mol

Ref: 54-PC1004141

2,3-DICHLORO-6,7-DIFLUOROQUINOXALINE

CAS: 91895-30-6

Formula: C₈H₂Cl₂F₂N₂

Purity: 97.0%

Molecular weight: 235.01

Ref: 10-F301385

2,3-Dichloro-6,7-difluoroquinoxaline

CAS: 91895-30-6

2,3-Dichloro-6,7-difluoroquinoxaline is an amino compound that is used in pharmacological studies. It has a high affinity for the a1 adenosine receptor and can be used to study the physiological effects of adenosine. 2,3-Dichloro-6,7-difluoroquinoxaline is also used in syntheses of heterocycles. It has been shown to have a high selectivity for nitrogen containing compounds and amines. 2,3-Dichloro-6,7-difluoroquinoxaline belongs to the class of tricyclic compounds.

Formula: C₈H₂Cl₂F₂N₂

Purity: Min. 95%

Molecular weight: 235.01 g/mol

Ref: 3D-RDA89530