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SE 563

Product Name
SE 563
CAS No.
174819-21-7
Chemical Name
SE 563
Synonyms
SE 563;Efavirenz Impurity 15;Efavirenz N-Methoxybenzyl Impurity;(S)-6-Chloro-4-(cyclopropylethynyl)-1-(4-methoxybenzyl)-4-(trifluoromethyl)-1,4-dihydro-2H-benzo[d][;(4S)-6-Chloro-4-(2-cyclopropylethynyl)-1,4-dihydro-1-[(4-methoxyphenyl)methyl]-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one;2H-3,1-Benzoxazin-2-one, 6-chloro-4-(2-cyclopropylethynyl)-1,4-dihydro-1-[(4-methoxyphenyl)methyl]-4-(trifluoromethyl)-, (4S)-
CBNumber
CB42710064
Molecular Formula
C22H17ClF3NO3
Formula Weight
435.82
MOL File
174819-21-7.mol
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SE 563 Property

Melting point:
112-114°C
Boiling point:
529.9±50.0 °C(Predicted)
Density 
1.44±0.1 g/cm3(Predicted)
storage temp. 
Amber Vial, -20°C Freezer, Under inert atmosphere
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
-2.47±0.40(Predicted)
form 
Solid
color 
White to Off-White
Stability:
Light Sensitive
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
S211300
Product name
SE563
Packaging
10mg
Price
$185
Updated
2021/12/16
AK Scientific
Product number
4525CS
Product name
N-(4-Methoxybenzyl)efavirenz
Packaging
5mg
Price
$387
Updated
2021/12/16
AK Scientific
Product number
4525CS
Product name
N-(4-Methoxybenzyl)efavirenz
Packaging
10mg
Price
$536
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
72311
Product name
SE563
Packaging
10mg
Price
$650
Updated
2021/12/16
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SE 563 Chemical Properties,Usage,Production

Uses

SE 563 is used in the synthesis of an HIV-1 reverse trancriptase inhibitor, Efavirenz (E425000).

SE 563 Preparation Products And Raw materials

Raw materials

Preparation Products

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SE 563 Suppliers

China 20 India 2 United States 2 Global 24
Cato Research Chemicals Inc.
Tel
020-81215950 4000-868-328
Email
customer@uwalab.com
Country
United States
ProdList
10404
Advantage
58
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80

174819-21-7, SE 563Related Search:

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

  • Efavirenz Impurity 15
  • Efavirenz N-Methoxybenzyl Impurity
  • (S)-6-Chloro-4-(cyclopropylethynyl)-1-(4-methoxybenzyl)-4-(trifluoromethyl)-1,4-dihydro-2H-benzo[d][
  • (4S)-6-Chloro-4-(2-cyclopropylethynyl)-1,4-dihydro-1-[(4-methoxyphenyl)methyl]-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one
  • 2H-3,1-Benzoxazin-2-one, 6-chloro-4-(2-cyclopropylethynyl)-1,4-dihydro-1-[(4-methoxyphenyl)methyl]-4-(trifluoromethyl)-, (4S)-
  • SE 563
  • 174819-21-7