1448-87-9 | 2-Chloroquinoxaline

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$9.00	$7.00
10g	98%	in stock	$11.00	$8.00
25g	98%	in stock	$23.00	$17.00
100g	98%	in stock	$91.00	$64.00

Description

• Catalog Number: AA72645
• Chemical Name: 2-Chloroquinoxaline
• CAS Number: 1448-87-9
• Molecular Formula: C8H5ClN2
• Molecular Weight: 164.5917
• MDL Number: MFCD00043907
• SMILES: Clc1cnc2c(n1)cccc2
• NSC Number: 43553

Computed Properties

• Complexity: 140
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 2.2

Upstream Synthesis Route

2-Chloroquinoxaline is a valuable building block used in chemical synthesis for various applications. With its unique structure and reactivity, this compound serves as a versatile intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its incorporation into organic molecules can impart specific functional properties and enhance the biological activity of the final products. Additionally, 2-Chloroquinoxaline can participate in diverse organic reactions such as substitution, coupling, and cyclization, thereby enabling the rapid and efficient synthesis of complex molecular structures. In medicinal chemistry, this compound has been employed in the development of novel drug candidates and bioactive compounds due to its ability to modulate molecular interactions and biological pathways. Its utility in advanced chemical synthesis makes 2-Chloroquinoxaline a valuable tool for researchers and professionals in the field of organic chemistry.

Literature

• 2-(3-Nitro-phen-oxy)quinoxaline.

  Acta crystallographica. Section E, Structure reports online 20100901

• 1-Naphthyl quinoxalin-2-yl ether.

  Acta crystallographica. Section E, Structure reports online 20090401

• 2-Naphthyl quinoxalin-2-yl ether.

  Acta crystallographica. Section E, Structure reports online 20090401

• 2-Chloro-quinoxaline.

  Acta crystallographica. Section E, Structure reports online 20090301

• Phenyl quinoxalin-2-yl ether.

  Acta crystallographica. Section E, Structure reports online 20080901

• Quinoxalin-2-yl o-tolyl ether.

  Acta crystallographica. Section E, Structure reports online 20080901

• Quinoxalin-2-yl m-tolyl ether.

  Acta crystallographica. Section E, Structure reports online 20080901

• Quinoxalin-2-yl p-tolyl ether.

  Acta crystallographica. Section E, Structure reports online 20080901

• Synthesis of 3-benzyl-2-substituted quinoxalines as novel monoamine oxidase A inhibitors.

  Bioorganic & medicinal chemistry letters 20060315

• Preparation of nitrogen-containing pi-deficient heteroaromatic Grignard reagents: oxidative magnesiation of nitrogen-containing pi-deficient halogenoheteroaromatics using active magnesium.

  The Journal of organic chemistry 20030307

• Synthesis of new arylaminoquinoxalines and their antimalarial activity in mice.

  The Journal of pharmacy and pharmacology 20011001