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21083-47-6,MFCD00005278
Catalog No.:AA00BDXC

21083-47-6 | 5,5-DIPHENYL-2-THIOHYDANTOIN

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Purity
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Price(USD)
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250mg
99%
in stock  
$42.00   $29.00
- +
1g
99%
in stock  
$65.00   $45.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00BDXC
Chemical Name:
5,5-DIPHENYL-2-THIOHYDANTOIN
CAS Number:
21083-47-6
Molecular Formula:
C15H12N2OS
Molecular Weight:
268.3336
MDL Number:
MFCD00005278
SMILES:
O=C1NC(=S)NC1(c1ccccc1)c1ccccc1
NSC Number:
82311
Properties
Computed Properties
 
Complexity:
352  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  
XLogP3:
3.1  

Literature

Title: A rapid and efficient ultrasound-assisted synthesis of 5,5-diphenylhydantoins and 5,5-diphenyl-2-thiohydantoins.

Journal: Ultrasonics sonochemistry 20110301

Title: Design and synthesis of an androgen receptor pure antagonist (CH5137291) for the treatment of castration-resistant prostate cancer.

Journal: Bioorganic & medicinal chemistry 20101201

Title: Anti-angiogenic action of 5,5-diphenyl-2-thiohydantoin-N10 (DPTH-N10).

Journal: Cancer letters 20081128

Title: Three modified activated carbons by different ligands for the solid phase extraction of copper and lead.

Journal: Journal of hazardous materials 20080415

Title: Structure and anti-proliferation function of 5,5-diphenyl-2-thiohydantoin (DPTH) derivatives in vascular endothelial cells.

Journal: Vascular pharmacology 20080101

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

Title: Substituted 2-thioxoimidazolidin-4-ones and imidazolidine-2,4-diones as fatty acid amide hydrolase inhibitors templates.

Journal: Journal of medicinal chemistry 20060112

Title: Anti-proliferation effect of 5,5-diphenyl-2-thiohydantoin (DPTH) in human vascular endothelial cells.

Journal: Biochemical pharmacology 20040101

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