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Efavirenz AMino Alcohol Ethyl CarbaMate

Product Name
Efavirenz AMino Alcohol Ethyl CarbaMate
CAS No.
211563-41-6
Chemical Name
Efavirenz AMino Alcohol Ethyl CarbaMate
Synonyms
Efavirenz impurity L;Efavirenz Impurity 9;Efavirenz Impurity 17;BZIKLWWRUOKZMC-HNNXBMFYSA-N;Efavirenz amino alcohol ethylcarbomate;Efavirenz AMino Alcohol Ethyl CarbaMate;Efavirenz Amino Alcohol Ethyl Carbamate (USP);Ethyl [4-Chloro-2-((1S)-1-trifluoromethyl-1-hydroxy-3- cyclopropyl-2-propyn-1-yl)phenyl]carbamate;Carbamic acid, N-[4-chloro-2-[(1S)-3-cyclopropyl-1-hydroxy-1-(trifluoromethyl)-2-propyn-1-yl]phenyl]-, ethyl ester
CBNumber
CB42709963
Molecular Formula
C16H15ClF3NO3
Formula Weight
361.74
MOL File
211563-41-6.mol
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Efavirenz AMino Alcohol Ethyl CarbaMate Property

Melting point:
138-140°C
storage temp. 
Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
color 
White
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
E425015
Product name
EfavirenzAminoAlcoholEthylCarbamate
Packaging
100mg
Price
$1695
Updated
2021/12/16
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Efavirenz AMino Alcohol Ethyl CarbaMate Chemical Properties,Usage,Production

Uses

Efavirenz Amino Alcohol Ethyl Carbamate is used in the synthesis of Efavirenz (E425000), a potent non-nucleoside HIV-1 reverse transcriptase inhibitor. Antiviral

Efavirenz AMino Alcohol Ethyl CarbaMate Preparation Products And Raw materials

Raw materials

Preparation Products

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Efavirenz AMino Alcohol Ethyl CarbaMate Suppliers

China 20 India 4 United States 2 Global 26

211563-41-6, Efavirenz AMino Alcohol Ethyl CarbaMateRelated Search:

Efavirenz 13C6 RAC 8-HYDROXY EFAVIRENZ Efavirenz (S)-1-(2-Amino-5-chlorophenyl)-1-(trifluoromethyl)-3-cyclopropyl-2-propyn-1-ol (S)-5-chloro-a-(Cyclopropylacetenyl)-2-[((4-methoxyphenyl)methyl)amino]-a- (trifluoromethyl) benzenemethanol (E-4) L 741211 rac 8-Hydroxy Efavirenz 6-chloro-4-[2-(2-methylcyclopropyl)ethynyl]-4-(trifluoromethyl)-1H-3,1-benzoxazin-2-one rac 8,14-Dihydroxy Efavirenz rac N-[4-Chloro-2-[3-cyclopropyl-1-hydroxy-1-(trifluoromethyl)\n-2-propynyl]phenyl]-4-methoxybenzamide Efavirenz Related Compound C (20 mg) (6-chloro-2-cyclopropyl-4-(trifluoromethyl)quinoline) L 743725 (4S)-6-Chloro-4-(cyclopropylethynyl)-1,4-dihydro-2-(4-methoxyphenyl)-4-(trifluoromethyl)-2H-3,1-benzoxazine (Mixture of 2 Diastereomers) rac Methyl Efavirenz [4-Chloro-2-[(1S)-3-cyclopropyl-1-hydroxy-1-(trifluoromethyl)-2-propynyl)phenyl]carbamic Acid Methyl Ester (S)-2-(2-AMINO-5-CHLOROPHENYL)-4-CYCLOPROPYL-1,1,1-TRIFLUOROBUT-3-YN-2-OL SE 563 Efavirenz Related Compound B (15 mg) ((S,E)-6-Chloro-4-(2-Cyclopropylvinyl)-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one)

  • Efavirenz AMino Alcohol Ethyl CarbaMate
  • BZIKLWWRUOKZMC-HNNXBMFYSA-N
  • Efavirenz Impurity 9
  • Efavirenz Amino Alcohol Ethyl Carbamate (USP)
  • Efavirenz amino alcohol ethylcarbomate
  • Efavirenz Impurity 17
  • Carbamic acid, N-[4-chloro-2-[(1S)-3-cyclopropyl-1-hydroxy-1-(trifluoromethyl)-2-propyn-1-yl]phenyl]-, ethyl ester
  • Ethyl [4-Chloro-2-((1S)-1-trifluoromethyl-1-hydroxy-3- cyclopropyl-2-propyn-1-yl)phenyl]carbamate
  • Efavirenz impurity L
  • 211563-41-6
  • C16H15ClF3NO3