Phenyl vinyl sulfide - CAS 1822-73-7

Name: Phenyl vinyl sulfide
Brand: BOC Sciences
Rating: 5 (1 reviews)

Catalog:	BB013901
Product Name:	Phenyl vinyl sulfide
CAS:	1822-73-7
Synonyms:	ethenylsulfanylbenzene

Technical Data

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Computed Properties

IUPAC Name:	ethenylsulfanylbenzene
Description:	Phenyl vinyl sulfide (CAS# 1822-73-7) is a useful research chemical.
Molecular Weight:	136.21
Molecular Formula:	C8H8S
Canonical SMILES:	C=CSC1=CC=CC=C1
InChI:	InChI=1S/C8H8S/c1-2-9-8-6-4-3-5-7-8/h2-7H,1H2
InChI Key:	GMPDOIGGGXSAPL-UHFFFAOYSA-N
Boiling Point:	94-95 °C (25 mmHg)
Purity:	98 %
Density:	1.042 g/cm³
MDL:	MFCD00009646
LogP:	2.92220

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Related Functional Groups

Sulfur Compounds

[2006276-82-8]C9H12ClNO4S2
[3-(N,N-Dimethylsulfamoyl)phenyl]methanesulfonyl Chloride
[85-47-2]C10H8O3S
1-Naphthalenesulfonic acid
[71996-48-0]C14H14O2S
1-Methyl-2-[(phenylsulfonyl)methyl]benzene
[162894-76-0]C2H7NO3S
2-Hydroxyethane-1-sulfonamide
[1005626-64-1]C13H14N6OS
3-(1,3-Dimethylpyrazol-4-yl)-5-[(1-methylpyrazol-4-yl)methylidene]-2-sulfanylideneimidazolidin-4-one
[72799-34-9]C11H12N2O2S
3-(2-Ethoxyphenyl)-2-Thioxoimidazolidin-4-One

GHS Hazard Statement:	H226 (100%): Flammable liquid and vapor [Warning Flammable liquids]
Precautionary Statement:	P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, and P501
Signal Word:	Warning

Publication Number	Title	Priority Date
CN-112886052-A	Composite electrolyte material, preparation method thereof and quasi-solid battery	20210312
CN-111592497-A	Method for preparing N-phenyl-4-benzenesulfonyl imidazole compound by copper catalysis	20200529
WO-2021209698-A1	Two-component composition, and uses thereof	20200416
WO-2021209699-A1	Process for polymerizing at least one radically polymerizable compound	20200416
WO-2021193786-A1	6-(fluoroalkyl)-3,4-dihydro-2h-pyran-5-carboxylic acid ester derivative, method for producing derivative, method for producing 2-(fluoroalkyl)nicotinic acid ester derivative, and method for producing 2-(fluoroalkyl)nicotinic acid derivative	20200327

PMID	Publication Date	Title	Journal
22823567	20120801	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
19199660	20090220	Efficient synthesis and subsequent transformations of phenylsulfanylbicyclo[2.2.2]octenones and phenylselenylbicyclo[2.2.2]octenones	The Journal of organic chemistry
18278931	20080320	Tin-free generation of alkyl radicals from alkyl 4-pentynyl sulfides via homolytic substitution at the sulfur atom	Organic letters
16477810	20051201	Analogs of squalene and oxidosqualene inhibit oxidosqualene cyclase of Trypanosoma cruzi expressed in Saccharomyces cerevisiae	Lipids
15609944	20041224	Total synthesis of the Kopsia lapidilecta alkaloid (+/-)-lapidilectine B	The Journal of organic chemistry

Complexity:	82.6
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	136.03467143
Formal Charge:	0
Heavy Atom Count:	9
Hydrogen Bond Acceptor Count:	1
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	136.03467143
Rotatable Bond Count:	2
Topological Polar Surface Area:	25.3 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	3.2