63547-13-7

  • Product Name:Acetamide,2-[(diphenylmethyl)sulfinyl]-N-hydroxy-
  • Molecular Formula:C15H15NO3S
  • Purity:99%
  • Molecular Weight:
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Product Details

Appearance:White, hygroscopic powder.

Adrafinil 63547-13-7 Phenylpiracetam for sale, Good Supplier In China

  • Molecular Formula:C15H15NO3S
  • Molecular Weight:289.355
  • Appearance/Colour:White, hygroscopic powder. 
  • Melting Point:150-160 °C 
  • Refractive Index:1.652 
  • PKA:8.22±0.20(Predicted) 
  • PSA:85.61000 
  • Density:1.342 g/cm3 
  • LogP:3.28670 

Adrafinil 63547-13-7 Usage

Analogues of adrafinil include modafinil, armodafinil, CRL-40,940, CRL-40,941, and fluorenol. It has effects similar to modafinil, which is a prescription drug that is used to treat narcolepsy. Adrafinil, 2-((diphenylmethyl)sulfinyl)-N-hydroxyacetamide, is a drug designed for the treatment of narcolepsy by promoting an awakened state, and to treat alertness and neurological symptoms in the elderly. Adrafinil is a research chemical that’s touted for its potential applications as a nootropic. 

InChI:InChI=1/C15H15NO3S/c17-14(16-18)11-20(19)15(12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,15,18H,11H2,(H,16,17)

63547-13-7 Relevant articles

Oral administration of adrafinil improves discrimination learning in aged beagle dogs.

NW Milgram,CT Siwak,P Gruet,P Atkinson,H Callahan

, Pharmacology Biochemistry & Behavior June 2000

An effect of adrafinil on motivation may partially account for these findings; however, adrafinil did not significantly affect response latency. Adrafinil is believed to serve as an alpha-1 adrenoceptor agonist.

Synthesis and determination of the absolute configuration of the enantiomers of modafinil

Prisinzano, Thomas,Podobinski, John,Tidgewell, Kevin,Luo, Min,Swenson, Dale

, p. 1053 - 1058 (2007/10/03)

The asymmetric synthesis of both enantiomers of modafinil, a unique CNS stimulant with a reduced abuse liability, is described. This approach effectively prepares modafinil on a multigram scale in several steps from benzhydrol. The described synthetic route has also been used to produce the more water soluble analogue, adrafinil. X-ray crystallographic analysis on (-)-(diphenylmethanesulfinyl)acetic acid has determined the absolute configuration to be R.

63547-13-7 Process route

2-benzhydrylsulfanyl-N-hydroxyacetamide
63547-44-4

2-benzhydrylsulfanyl-N-hydroxyacetamide

adrafinil
63547-13-7

adrafinil

Conditions
Conditions Yield
With dihydrogen peroxide; acetic acid; at 40 ℃;
72%
1,1-Diphenylmethanol
91-01-0

1,1-Diphenylmethanol

adrafinil
63547-13-7

adrafinil

Conditions
Conditions Yield
Multi-step reaction with 4 steps
1: 99 percent / trifluoroacetic acid / 3 h / 20 °C
2: 99 percent / H2SO4 / Heating
3: 92 percent / hydroxylamine hydrochloride; KOH / methanol / 0.25 h
4: 72 percent / aq. H2O2; acetic acid / 40 °C
With potassium hydroxide; sulfuric acid; hydroxylamine hydrochloride; dihydrogen peroxide; acetic acid; trifluoroacetic acid; In methanol;
 

63547-13-7 Upstream products

  • 63547-44-4
    63547-44-4

    2-benzhydrylsulfanyl-N-hydroxyacetamide

  • 91-01-0
    91-01-0

    1,1-Diphenylmethanol

  • 63547-22-8
    63547-22-8

    (benzhydrylthio)acetic acid

  • 63547-23-9
    63547-23-9

    (diphenylmethyl)(ethyl acetate)sulfide

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