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831-91-4,MFCD00003066
Catalog No.:AA003O1S

831-91-4 | BENZYL PHENYL SULFIDE

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%(GC)
in stock  
$24.00   $17.00
- +
10g
>98.0%(GC)
in stock  
$38.00   $27.00
- +
25g
99%
in stock  
$50.00   $35.00
- +
100g
99%
in stock  
$122.00   $85.00
- +
500g
99%
in stock  
$436.00   $305.00
- +
  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003O1S
Chemical Name:
BENZYL PHENYL SULFIDE
CAS Number:
831-91-4
Molecular Formula:
C13H12S
Molecular Weight:
200.2994
MDL Number:
MFCD00003066
SMILES:
c1ccc(cc1)SCc1ccccc1
NSC Number:
56472
Properties
Properties
 
BP:
321.1°C at 760 mmHg  
Form:
Solid  
MP:
40-44 °C(lit.)  
Refractive Index:
1.6170 (estimate)  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
143  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
3.9  

Literature

Title: Recent advances in the synthesis of raloxifene: a selective estrogen receptor modulator.

Journal: European journal of medicinal chemistry 20120501

Title: The oxidative properties of a manganese(IV) hydroperoxide moiety and its relationships with the corresponding manganese(IV) oxo and hydroxo moieties.

Journal: Dalton transactions (Cambridge, England : 2003) 20120307

Title: Integration of on-column catalysis and EKC analysis: investigation of enantioselective sulfoxidations.

Journal: Electrophoresis 20120301

Title: 2-Benzyl-sulfanyl-4-pentyl-6-(phenyl-sulfan-yl)pyrimidine-5-carbonitrile.

Journal: Acta crystallographica. Section E, Structure reports online 20111101

Title: Novel fungicidal benzylsulfanyl-phenylguanidines.

Journal: Bioorganic & medicinal chemistry letters 20110615

Title: Inhibitory effects on microbial growth using the derivatives of benzyl phenyl sulfide.

Journal: Biocontrol science 20110601

Title: Studies on the reactive species in fluoride-mediated carbon-carbon bond-forming reactions: carbanion formation by desilylation with fluoride and enolates.

Journal: The Journal of organic chemistry 20060526

Title: Inhibition of histidine ammonia lyase by heteroaryl-alanines and acrylates.

Journal: Chemistry & biodiversity 20060501

Title: The interaction of heteroaryl-acrylates and alanines with phenylalanine ammonia-lyase from parsley.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20060320

Title: Catalysis of oxo transfer to prochiral sulfides by oxovanadium(v) compounds that model the active center of haloperoxidases.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20031006

Title: Mechanism of the oxidation of aromatic sulfides catalysed by a water soluble iron porphyrin.

Journal: Organic & biomolecular chemistry 20030121

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