(S)-5-[(4-hydroxyphenyl)methyl]-3-phenyl-2-thioxoimidazolidin-4-one

  • CasNo：29588-08-7
  • purity：99%
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Details

Factory Export Top Purity (S)-5-[(4-hydroxyphenyl)methyl]-3-phenyl-2-thioxoimidazolidin-4-one 29588-08-7 In Stock

  • Molecular Formula: C16H14 N2 O2 S
  • Molecular Weight: 298.365
  • Vapor Pressure: 2.37E-09mmHg at 25°C 
  • Boiling Point: 467.2°Cat760mmHg 
  • Flash Point: 236.4°C 
  • PSA： 91.70000 
  • Density: 1.41g/cm3 
  • LogP: 2.13650 

(S)-5-[(4-hydroxyphenyl)methyl]-3-phenyl-2-thioxoimidazolidin-4-one(Cas 29588-08-7) Usage

General Description

(S)-5-[(4-hydroxyphenyl)methyl]-3-phenyl-2-thioxoimidazolidin-4-one is a chemical compound with a complex molecular structure. It consists of a five-membered imidazolidin-4-one ring with a thioxo group and a phenyl group attached at different positions. The compound also contains a (4-hydroxyphenyl)methyl group, which adds to its complexity. This chemical may have potential pharmaceutical applications due to its structure and functional groups, but further research is needed to determine its specific uses and properties.

InChI:InChI=1/C16H14N2O2S/c19-13-8-6-11(7-9-13)10-14-15(20)18(16(21)17-14)12-4-2-1-3-5-12/h1-9,14,19H,10H2,(H,17,21)

29588-08-7 Relevant articles

Modulation of the pharmacological activities of secretory phospholipase A2 from Crotalus durissus cascavella induced by naringin

Santos, Marcelo L.,Toyama, Daniela O.,Oliveira, Simone C. B.,Cotrim, Camila A.,Diz-Filho, Eduardo B. S.,Fagundes, Fabio H. R.,Soares, Veronica C. G.,Aparicio, Ricardo,Toyama, Marcos H.

experimental part, p. 738 - 761 (2011/04/15)

In this work we have characterized the a...

29588-08-7 Process route

phenyl thioisocyanate
49645-33-2

phenyl thioisocyanate

secretory phospholipase A2 from Crotalus durissus cascavella venom modified with naringin

secretory phospholipase A2 from Crotalus durissus cascavella venom modified with naringin

3-phenyl-2-thioxoimidazolidin-4-one
2010-15-3

3-phenyl-2-thioxoimidazolidin-4-one

hexahydro-2-phenyl-3-thioxopyrrolo[1,2-c]imidazol-1-one
29635-99-2

hexahydro-2-phenyl-3-thioxopyrrolo[1,2-c]imidazol-1-one

C<sub>13</sub>H<sub>12</sub>N<sub>4</sub>OS

C13 H12 N4 OS

(<i>S</i>)-5-(4-hydroxy-benzyl)-3-phenyl-2-thioxo-imidazolidin-4-one
29588-08-7

(S )-5-(4-hydroxy-benzyl)-3-phenyl-2-thioxo-imidazolidin-4-one

5-(hydroxymethyl)-3-phenyl-2-thioxoimidazolidin-4-one
29635-84-5

5-(hydroxymethyl)-3-phenyl-2-thioxoimidazolidin-4-one

2-(5-oxo-1-phenyl-2-thioxoimidazolidin-4-yl)acetic acid
29588-04-3

2-(5-oxo-1-phenyl-2-thioxoimidazolidin-4-yl)acetic acid

L-arginine N-phenylthiohydantoin
29635-93-6

L-arginine N-phenylthiohydantoin

(S)-5-methyl-3-phenyl-2-thioxoimidazolidin-4-one
7390-20-7

(S)-5-methyl-3-phenyl-2-thioxoimidazolidin-4-one

3-(5-oxo-1-phenyl-2-thioxoimidazolidin-4-yl)propanoic acid
7390-22-9

3-(5-oxo-1-phenyl-2-thioxoimidazolidin-4-yl)propanoic acid

5-(1-hydroxyethyl)-3-phenyl-2-thioxoimidazolidin-4-one

5-(1-hydroxyethyl)-3-phenyl-2-thioxoimidazolidin-4-one

Conditions
Conditions Yield
secretory phospholipase A2 from Crotalus durissus cascavella venom modified with naringin; With hydrogenchloride; phenol; In water; at 106 ℃; for 24h;
phenyl thioisocyanate; With triethylamine; In ethanol; water;
L-tyrosine
60-18-4,18875-48-4,25619-78-7,30704-25-7

L-tyrosine

phenyl isothiocyanate
103-72-0

phenyl isothiocyanate

(<i>S</i>)-5-(4-hydroxy-benzyl)-3-phenyl-2-thioxo-imidazolidin-4-one
29588-08-7

(S )-5-(4-hydroxy-benzyl)-3-phenyl-2-thioxo-imidazolidin-4-one

Conditions
Conditions Yield

29588-08-7 Upstream products

  • 60-18-4
    60-18-4

    L-tyrosine

  • 103-72-0
    103-72-0

    phenyl isothiocyanate

  • 49645-33-2
    49645-33-2

    phenyl thioisocyanate

29588-08-7 Downstream products

  • 67120-03-0
    67120-03-0

    (S)-3-(4-Hydroxy-phenyl)-N-methyl-2-(3-phenyl-thioureido)-propionamide

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