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allyl phenyl sulfide
(allylthio)benzene

Supplier Sponsors

CAS Number: 5296-64-0Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:226-142-5
FDA UNII: PZD2SYT8MG
Nikkaji Web:J297.984E
Beilstein Number:1856940
MDL:MFCD00014957
XlogP3:3.50 (est)
Molecular Weight:150.24370000
Formula:C9 H10 S
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:information only not used for fragrances or flavors
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
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Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 208.39 °C. @ 760.00 mm Hg (est)
Vapor Pressure:0.098000 mmHg (est)
Flash Point: 174.00 °F. TCC ( 78.80 °C. ) (est)
logP (o/w): 3.510
Soluble in:
 alcohol
 water, 76.12 mg/L @ 25 °C (est)
Insoluble in:
 water
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
Allyl phenyl sulfide
Endeavour Specialty Chemicals
Allyl phenyl sulphide
Speciality Chemical Product Groups
Robinson Brothers
Allyl phenyl sulphide
https://www.robinsonbrothers.uk/chemistry-competences
Santa Cruz Biotechnology
For experimental / research use only.
Allyl phenyl sulfide
Sigma-Aldrich
For experimental / research use only.
Allyl Phenyl Sulfide ≥96.5% (GC)
TCI AMERICA
For experimental / research use only.
Allyl Phenyl Sulfide >98.0%(GC)
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
information only not used for fragrances or flavors
IFRA Purity Specification: < 0.1% free allyl alcohol
Recommendation for allyl phenyl sulfide usage levels up to:
 not for fragrance use.
 
Recommendation for allyl phenyl sulfide flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :79180
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
prop-2-enylsulfanylbenzene
Chemidplus:0005296640
 
References:
 prop-2-enylsulfanylbenzene
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):79180
Pubchem (sid):135035176
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2930.90.2900
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 allyl sulfanyl benzene
(allyl thio) benzene
(allylsulfanyl)benzene
(allylthio)benzene
 benzene, (2-propen-1-ylthio)-
(prop-2-en-1-ylsulfanyl)benzene
 prop-2-enylsulfanylbenzene
 prop-2-enylthiobenzene
(2-propenylthio)benzene
 

Articles:

PubMed:Regio- and enantioselective iridium-catalyzed allylation of thiophenol: synthesis of enantiopure allyl phenyl sulfides.
PubMed:Readily prepared 3-chloro-1-(phenylthio)propene, a versatile three-carbon annulating agent.
PubMed:Thiomaleic anhydride: a convenient building block for the synthesis of alpha-substituted gamma- and delta-lactones through free-radical addition, nucleophilic ring opening, and subsequent thiocarboxylate manipulation.
PubMed:2-Phenylthio-3-bromopropene, a valuable synthon, easily prepared by a simple rearrangement.
PubMed:Screening of organosulfur compounds as inhibitors of human CYP2A6.
PubMed:The magnesium-ene cyclization stereochemically directed by an allylic oxyanionic group and its application to a highly stereoselective synthesis of (+/-)-matatabiether. Allylmagnesium compounds by reductive magnesiation of allyl phenyl sulfides.
PubMed:Claisen rearrangement of allyl phenyl ether and its sulfur and selenium analogues on electron impact
PubMed:Asymmetric copper-catalyzed
 
Notes:
None found
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