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Home Sulfos Phenyl vinyl sulfoxide

Phenyl vinyl sulfoxide

CAS No.:
20451-53-0
Catalog Number:
AG0029J7
Molecular Formula:
C8H8OS
Molecular Weight:
152.2135
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$175
- +
25g
95%
In Stock USA
United States
$563
- +
Product Description
Catalog Number:
AG0029J7
Chemical Name:
Phenyl vinyl sulfoxide
CAS Number:
20451-53-0
Molecular Formula:
C8H8OS
Molecular Weight:
152.2135
MDL Number:
MFCD00002086
IUPAC Name:
ethenylsulfinylbenzene
InChI:
InChI=1S/C8H8OS/c1-2-10(9)8-6-4-3-5-7-8/h2-7H,1H2
InChI Key:
MZMJHXFYLRTLQX-UHFFFAOYSA-N
SMILES:
C=CS(=O)c1ccccc1
EC Number:
243-831-6
Properties
Complexity:
136  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
152.03g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
152.211g/mol
Monoisotopic Mass:
152.03g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
36.3A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
1.1  
Literature
Title Journal
Probing the formation of bicyclo[4.2.0]octan-1-ols. The Journal of organic chemistry 20040820
Diels-Alder reactions of 4-triflyloxy-2,6,6-trimethyl-2,4-cyclohexadienone. An expedient methodology for the synthesis of bicyclo[2.2.2]oct-5-en-2-ones and bicyclo[2.2.2]octa-5,7-dien-2-ones. The Journal of organic chemistry 20040123
The formation of bicyclo[n.2.0]alkan-1-ols from the reaction of the lithium enolates of simple ketones and phenyl vinyl sulfoxide. Organic & biomolecular chemistry 20030421
Lead discovery of alpha,beta-unsaturated sulfones from a combinatorial library as inhibitors of inducible VCAM-1 expression. Bioorganic & medicinal chemistry letters 20030224
Properties