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(5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazol-4-yl)methanol

Detailed Information

  • Product Name:(5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazol-4-yl)methanol
  • CasNo.:946426-89-7
  • MF:C13H11Cl2NO2
  • MW:284.142

pd_nature

  • Purity:99%
  • pd_boiling:
  • Packing:
  • Throughput:

Product Details;

CasNo: 946426-89-7

MF: C13H11Cl2NO2

Factory supply (5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazol-4-yl)methanol 946426-89-7 with sufficient production capacity

  • Molecular Formula:C13H11Cl2NO2
  • Molecular Weight:284.142
  • PSA:46.26000 
  • LogP:4.01810 

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946426-89-7 Process route

ethyl 5-cyclopropyl-3-(2,6-dichlorophenyl)-1,2-oxazole-4-carboxylate
1020569-65-6

ethyl 5-cyclopropyl-3-(2,6-dichlorophenyl)-1,2-oxazole-4-carboxylate

4-(hydroxymethyl)-5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazole
946426-89-7

4-(hydroxymethyl)-5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazole

Conditions
Conditions Yield
ethyl 5-cyclopropyl-3-(2,6-dichlorophenyl)-1,2-oxazole-4-carboxylate; With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 5.5h;
With water; rochelle salt; In tetrahydrofuran; toluene;
96%
With diisobutylaluminium hydride; In tetrahydrofuran; at -70 - 20 ℃; for 16h;
89%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; for 2h;
78%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 2h; Inert atmosphere;
78%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 25 ℃;
75%
With diisobutylaluminium hydride; In tetrahydrofuran; at 0 - 20 ℃; for 7h;
60%
With diisobutylaluminium hydride; In tetrahydrofuran; at 0 - 20 ℃; for 7h;
60%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; for 2h;
36%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; for 2h;
36%
ethyl 5-cyclopropyl-3-(2,6-dichlorophenyl)-1,2-oxazole-4-carboxylate; With diisobutylaluminium hydride; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
With hydrogenchloride; water; In tetrahydrofuran; methanol;
With diisobutylaluminium hydride; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazole-4-carboxylic acid methyl ester
946426-88-6

5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazole-4-carboxylic acid methyl ester

4-(hydroxymethyl)-5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazole
946426-89-7

4-(hydroxymethyl)-5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazole

Conditions
Conditions Yield
With diisobutylaluminium hydride; In tetrahydrofuran; at 20 ℃; for 2h;
96%
5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazole-4-carboxylic acid methyl ester; With diisobutylaluminium hydride; In tetrahydrofuran; toluene; for 2h;
With hydrogenchloride; sodium hydroxide; water; In tetrahydrofuran; toluene;
93%
5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazole-4-carboxylic acid methyl ester; With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 ℃; for 2h;
With hydrogenchloride; water; In tetrahydrofuran; toluene; Product distribution / selectivity;
93%
With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 2h;
92%
With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 2h;
92%
With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 2h;
92%
With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 2h;
92%
5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazole-4-carboxylic acid methyl ester; With diisobutylaluminium hydride; In dichloromethane; toluene; at -5 - 25 ℃; for 3.5h;
With hydrogenchloride; water; In dichloromethane; toluene; at 8 - 10 ℃; for 0.5h; Product distribution / selectivity;
90%
With lithium aluminium tetrahydride; In tetrahydrofuran; at -10 - 20 ℃; for 0.5h;
90%
5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazole-4-carboxylic acid methyl ester; With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 2h;
With methanol; In tetrahydrofuran; toluene; at 0 ℃; for 0.166667h; Product distribution / selectivity;
85%
With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 2h;
85%
With diisobutylaluminium hydride; In tetrahydrofuran; at 0 - 20 ℃; for 2h;
84.2%
With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 2h; Inert atmosphere;
83%
With lithium aluminium tetrahydride; In tetrahydrofuran; at -10 ℃; Inert atmosphere;
60%
With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 2h;
8.46 g
With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 2h;
8.46 g
With diisobutylaluminium hydride; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 6h;
With lithium aluminium tetrahydride; In tetrahydrofuran; at -10 ℃; for 3h;

946426-89-7 Upstream products

  • 1020569-65-6
    1020569-65-6

    ethyl 5-cyclopropyl-3-(2,6-dichlorophenyl)-1,2-oxazole-4-carboxylate

  • 946426-88-6
    946426-88-6

    5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazole-4-carboxylic acid methyl ester

  • 6579-27-7
    6579-27-7

    2,6-Dichloro-N-hydroxybenzenecarboximidoyl chloride

  • 83-38-5
    83-38-5

    2,6-dichlorobenzaldehyde

946426-89-7 Downstream products

  • 1020569-74-7
    1020569-74-7

    methyl 7-[4-({[5-cyclopropyl-3-(2,6-dichlorophenyl)-4-isoxazolyl]methyl}oxy)phenyl]-3-isoquinolinecarboxylate

  • 1020569-84-9
    1020569-84-9

    methyl 6-[4-({[5-cyclopropyl-3-(2,6-dichlorophenyl)-4-isoxazolyl]methyl}oxy)phenyl]-2-quinolinecarboxylate

  • 946426-94-4
    946426-94-4

    4-(bromomethyl)-5-cyclopropyl-3-(2,6-dichlorophenyl)-1,2-oxazole

  • 1198085-33-4
    1198085-33-4

    5-cyclopropyl-3-(2,6-dichlorophenyl)-4-((5-nitro-6-(trifluoromethyl)pyridin-2-yloxy)methyl) isoxazole

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