Keywords

• 2213-63-0
• 2,3-Dichloroquinoxaline
• 98% purity 2,3-Dichloroquinoxaline CAS 2213-63-0

Quick Details

• ProName: Manufacture Supply 98% purity 2,3-Dich...
• CasNo: 2213-63-0
• Molecular Formula: C8H4Cl2N2
• Appearance: off white to yellowish needles
• Application: only for research purpose
• DeliveryTime: 3 days after payment
• PackAge: 1kg/bag, 25kg/drum
• Port: any port
• ProductionCapacity: 300 Kilogram/Month
• Purity: 98% HPLC
• Storage: store at normal temperature, sealed fr...
• Transportation: normal shipment
• LimitNum: 1 Kilogram
• Related Substances: 2,3-Dichloroquinoxaline
• Residue on Ignition: <0.1%
• Heavy Metal: <20ppm
• Valid Period: 24months

Superiority

Wuhan Vanz Pharm Inc, supplying hih quality 2,3-Dichloroquinoxaline CAS 2213-63-0, with best price and stable supply.

2,3-Dichloroquinoxaline was used in the synthesis of mono and 2,3-disubstituted quinoxalines[3]. It was used in solid phase synthesis of HPLC chiral stationary phase containing the N,N′-dialkyl-2,3-diaminoquinoxaline group as a linking structure

2,3-Dichloroquinoxaline reacts with 6-aminothiouracil in ethanol/TEA to form 6-amino-2-(3-chloroquinoxalin-2-ylthio)pyrimidin-4(3H)-one[1]. It reacts with cholest-5-en-3-one semicarbazone/thiosemicarbazone to form steriodal cholest-5-en-3-oxazolo and thiazoloquinoxaline

2,3-Dichloroquinoxaline was used in the synthesis of mono and 2,3-disubstituted quinoxalines[3]. It was used in solid phase synthesis of HPLC chiral stationary phase containing the N,N′-dialkyl-2,3-diaminoquinoxaline group as a linking structure

2,3-Dichloroquinoxaline reacts with 6-aminothiouracil in ethanol/TEA to form 6-amino-2-(3-chloroquinoxalin-2-ylthio)pyrimidin-4(3H)-one[1]. It reacts with cholest-5-en-3-one semicarbazone/thiosemicarbazone to form steriodal cholest-5-en-3-oxazolo and thiazoloquinoxaline

2,3-Dichloroquinoxaline was used in the synthesis of mono and 2,3-disubstituted quinoxalines[3]. It was used in solid phase synthesis of HPLC chiral stationary phase containing the N,N′-dialkyl-2,3-diaminoquinoxaline group as a linking structure

2,3-Dichloroquinoxaline reacts with 6-aminothiouracil in ethanol/TEA to form 6-amino-2-(3-chloroquinoxalin-2-ylthio)pyrimidin-4(3H)-one[1]. It reacts with cholest-5-en-3-one semicarbazone/thiosemicarbazone to form steriodal cholest-5-en-3-oxazolo and thiazoloquinoxaline

2,3-Dichloroquinoxaline was used in the synthesis of mono and 2,3-disubstituted quinoxalines[3]. It was used in solid phase synthesis of HPLC chiral stationary phase containing the N,N′-dialkyl-2,3-diaminoquinoxaline group as a linking structure

2,3-Dichloroquinoxaline reacts with 6-aminothiouracil in ethanol/TEA to form 6-amino-2-(3-chloroquinoxalin-2-ylthio)pyrimidin-4(3H)-one[1]. It reacts with cholest-5-en-3-one semicarbazone/thiosemicarbazone to form steriodal cholest-5-en-3-oxazolo and thiazoloquinoxaline

Details

2,3-Dichloroquinoxaline was used in the synthesis of mono and 2,3-disubstituted quinoxalines[3]. It was used in solid phase synthesis of HPLC chiral stationary phase containing the N,N′-dialkyl-2,3-diaminoquinoxaline group as a linking structure

2,3-Dichloroquinoxaline reacts with 6-aminothiouracil in ethanol/TEA to form 6-amino-2-(3-chloroquinoxalin-2-ylthio)pyrimidin-4(3H)-one[1]. It reacts with cholest-5-en-3-one semicarbazone/thiosemicarbazone to form steriodal cholest-5-en-3-oxazolo and thiazoloquinoxaline

2,3-Dichloroquinoxaline was used in the synthesis of mono and 2,3-disubstituted quinoxalines[3]. It was used in solid phase synthesis of HPLC chiral stationary phase containing the N,N′-dialkyl-2,3-diaminoquinoxaline group as a linking structure

2,3-Dichloroquinoxaline reacts with 6-aminothiouracil in ethanol/TEA to form 6-amino-2-(3-chloroquinoxalin-2-ylthio)pyrimidin-4(3H)-one[1]. It reacts with cholest-5-en-3-one semicarbazone/thiosemicarbazone to form steriodal cholest-5-en-3-oxazolo and thiazoloquinoxaline