Efavirenz Impurity 15(8,14-Dihydroxy Efavirenz) Chemical Properties

solubility 

DMSO (Slightly), Methanol (Slightly)

form 

Solid

color 

Off-White to Pale Brown

Efavirenz Impurity 15(8,14-Dihydroxy Efavirenz) Usage And Synthesis

Uses

(S)-8,14-Dihydroxy Efavirenz, is a metabolite of Efavirenz (E425000), a nonnucleoside HIV-1 reverse transcriptase inhibitor. Antiviral.

Efavirenz Impurity 15(8,14-Dihydroxy Efavirenz)(252343-27-4)Related Product Information

• RAC 8-HYDROXY EFAVIRENZ
• Efavirenz
• Enantiomer Efavirenz
• (S)-5-chloro-a-(Cyclopropylacetenyl)-2-[((4-methoxyphenyl)methyl)amino]-a- (trifluoromethyl) benzenemethanol (E-4)
• [4-Chloro-2-[(1S)-3-cyclopropyl-1-hydroxy-1-(trifluoromethyl)-2-propynyl)phenyl]carbamic Acid Methyl Ester
• (S)-1-(2-Amino-5-chlorophenyl)-1-(trifluoromethyl)-3-cyclopropyl-2-propyn-1-ol
• (4S)-6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro-2-(4-methoxyphenyl)-4-(trifluoromethyl)-2H-3,1-benzoxazine_x000b_(Mixture of 2 Diastereomers)
• Efavirenz Impurity 13(7-Hydroxy Efavirenz)
• Efavirenz AMino Alcohol Ethyl CarbaMate
• Efavirenz Related Compound C (20 mg) (6-chloro-2-cyclopropyl-4-(trifluoromethyl)quinoline)
• rac 7-Hydroxy Efavirenz
• Efavirenz IP Impurity A
• Efavirenz Related Compound B (15 mg) ((S,E)-6-Chloro-4-(2-Cyclopropylvinyl)-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one)
• rac 8-Hydroxy Efavirenz
• rac 8,14-Dihydroxy Efavirenz