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2213-63-0 2,3-Dichloroquinoxaline 98% purity 2,3-Dichloroquinoxaline CAS 2213-63-0
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Name | 2,3-Dichloroquinoxaline |
CAS No. | 2213-63-0 |
Purity | 99% |
Appearance | Off white needles |
COA | Available |
MOQ | 1kg |
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
Name | 2,3-Dichloroquinoxaline |
CAS No. | 2213-63-0 |
Purity | 99% |
Appearance | Off white needles |
COA | Available |
MOQ | 1kg |
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
Name | 2,3-Dichloroquinoxaline |
CAS No. | 2213-63-0 |
Purity | 99% |
Appearance | Off white needles |
COA | Available |
MOQ | 1kg |
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
Name | 2,3-Dichloroquinoxaline |
CAS No. | 2213-63-0 |
Purity | 99% |
Appearance | Off white needles |
COA | Available |
MOQ | 1kg |
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
Name | 2,3-Dichloroquinoxaline |
CAS No. | 2213-63-0 |
Purity | 99% |
Appearance | Off white needles |
COA | Available |
MOQ | 1kg |
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
Name | 2,3-Dichloroquinoxaline |
CAS No. | 2213-63-0 |
Purity | 99% |
Appearance | Off white needles |
COA | Available |
MOQ | 1kg |
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
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