Home Other Building Blocks 1-Methyl-4-(methylsulphinyl)benzene

1-Methyl-4-(methylsulphinyl)benzene

CAS No.:
934-72-5
Catalog Number:
AG003EI0
Molecular Formula:
C8H10OS
Molecular Weight:
154.2294
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$88
- +
5g
95%
In Stock USA
United States
$350
- +
Product Description
Catalog Number:
AG003EI0
Chemical Name:
1-Methyl-4-(methylsulphinyl)benzene
CAS Number:
934-72-5
Molecular Formula:
C8H10OS
Molecular Weight:
154.2294
MDL Number:
MFCD00075175
IUPAC Name:
1-methyl-4-methylsulfinylbenzene
InChI:
InChI=1S/C8H10OS/c1-7-3-5-8(6-4-7)10(2)9/h3-6H,1-2H3
InChI Key:
FEVALTJSQBFLEU-UHFFFAOYSA-N
SMILES:
Cc1ccc(cc1)S(=O)C
NSC Number:
141186
Properties
Complexity:
125  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
154.045g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
154.227g/mol
Monoisotopic Mass:
154.045g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
36.3A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
1.4  
Literature
Title Journal
Precise and rapid detection of optical activity for accumulative femtosecond spectroscopy. Optics express 20120521
Oxidation of sulfoxides and arsenic(III) in corrosion of nanoscale zero valent iron by oxygen: evidence against ferryl ions (Fe(IV)) as active intermediates in Fenton reaction. Environmental science & technology 20110101
Imination of sulfides and sulfoxides with sulfonylimino-lambda3-bromane under mild, metal-free conditions. Chemistry (Weinheim an der Bergstrasse, Germany) 20100802
Role of ligands in permanganate oxidation of organics. Environmental science & technology 20100601
An efficient stereoselective synthesis of penaresidin a from (e)-2-protected amino-3,4-unsaturated sulfoxide. The Journal of organic chemistry 20100205
Contribution of the stereospecific methionine sulphoxide reductases MsrA and MsrB to oxidative and nitrosative stress resistance in the food-borne pathogen Campylobacter jejuni. Microbiology (Reading, England) 20080801
[Occupational exposure evaluation in some endoscopic services of Campania region sanitary structures]. Giornale italiano di medicina del lavoro ed ergonomia 20070101
Using enzyme inhibition as a high throughput method to measure the enantiomeric excess of a chiral sulfoxide. Organic letters 20051027
Cytochrome c-crown ether complexes as supramolecular catalysts: cold-active synzymes for asymmetric sulfoxide oxidation in methanol. Inorganic chemistry 20050221
Evaluation of peracetic acid permeation during flash sterilization through pharmaceutical plastic polymers used in cytotoxic reconstitution units. PDA journal of pharmaceutical science and technology 20050101
Simultaneous sampling of peroxyacetic acid and hydrogen peroxide in workplace atmospheres. The Annals of occupational hygiene 20041101
Dioxygenase-catalysed oxidation of alkylaryl sulfides: sulfoxidation versus cis-dihydrodiol formation. Organic & biomolecular chemistry 20040907
Catalysis of oxo transfer to prochiral sulfides by oxovanadium(v) compounds that model the active center of haloperoxidases. Chemistry (Weinheim an der Bergstrasse, Germany) 20031006
Chemical activation of cytochrome c proteins via crown ether complexation: cold-active synzymes for enantiomer-selective sulfoxide oxidation in methanol. Journal of the American Chemical Society 20030924
Aerobic oxidation of methyl p-tolyl sulfide catalyzed by a remarkably labile heteroscorpionate RuII-aqua complex, fac-[RuII(H2O)(dpp)(tppm)]2+. Journal of the American Chemical Society 20030115
Properties