Home Other Building Blocks Phenyl vinyl sulfide

Phenyl vinyl sulfide

CAS No.:
1822-73-7
Catalog Number:
AG0023H6
Molecular Formula:
C8H8S
Molecular Weight:
136.2141
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
Product Description
Catalog Number:
AG0023H6
Chemical Name:
Phenyl vinyl sulfide
CAS Number:
1822-73-7
Molecular Formula:
C8H8S
Molecular Weight:
136.2141
MDL Number:
MFCD00009646
IUPAC Name:
ethenylsulfanylbenzene
InChI:
InChI=1S/C8H8S/c1-2-9-8-6-4-3-5-7-8/h2-7H,1H2
InChI Key:
GMPDOIGGGXSAPL-UHFFFAOYSA-N
SMILES:
C=CSc1ccccc1
EC Number:
217-351-2
UNII:
253GML9Q62
NSC Number:
39625
Properties
Complexity:
82.6  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
136.035g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
136.212g/mol
Monoisotopic Mass:
136.035g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
25.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.2  
Literature
Title Journal
Z- and enantioselective ring-opening/cross-metathesis with enol ethers catalyzed by stereogenic-at-Ru carbenes: reactivity, selectivity, and Curtin-Hammett kinetics. Journal of the American Chemical Society 20120801
Efficient synthesis and subsequent transformations of phenylsulfanylbicyclo[2.2.2]octenones and phenylselenylbicyclo[2.2.2]octenones. The Journal of organic chemistry 20090220
Tin-free generation of alkyl radicals from alkyl 4-pentynyl sulfides via homolytic substitution at the sulfur atom. Organic letters 20080320
Analogs of squalene and oxidosqualene inhibit oxidosqualene cyclase of Trypanosoma cruzi expressed in Saccharomyces cerevisiae. Lipids 20051201
Total synthesis of the Kopsia lapidilecta alkaloid (+/-)-lapidilectine B. The Journal of organic chemistry 20041224
Properties