Ethylbenzene

Base Information

Chemical Name:Ethylbenzene
CAS No.:79637-11-9
Molecular Formula:C8H8
Molecular Weight:104.14900
Hs Code.:
European Community (EC) Number:202-849-4,616-714-6
ICSC Number:0268
NSC Number:406903
UN Number:1175
UNII:L5I45M5G0O
DSSTox Substance ID:DTXSID3020596
Nikkaji Number:J2.272.471A,J3.192.069H,J3.589K
Wikipedia:Ethylbenzene
Wikidata:Q409184,Q83038858,Q83048382
NCI Thesaurus Code:C173418
Metabolomics Workbench ID:50380
ChEMBL ID:CHEMBL371561
Mol file:79637-11-9.mol

Synonyms:ethylbenzene

Suppliers and Price of Ethylbenzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 17 raw suppliers

Chemical Property of Ethylbenzene

Chemical Property:

Melting Point:-31oC
Boiling Point:145oC
PSA：0.00000
LogP:2.32960
XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:106.078250319
Heavy Atom Count:8
Complexity:51.1
Transport DOT Label:Flammable Liquid

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Solvents -> Aromatic Solvents
Canonical SMILES:CCC1=CC=CC=C1
Inhalation Risk:A harmful contamination of the air will be reached rather slowly on evaporation of this substance at 20 °C.
Effects of Short Term Exposure:The substance is irritating to the eyes, skin and respiratory tract. If this liquid is swallowed, aspiration into the lungs may result in chemical pneumonitis. The substance may cause effects on the central nervous system. Exposure above the OEL could cause lowering of consciousness.
Effects of Long Term Exposure:This substance is possibly carcinogenic to humans. The substance may have effects on the kidneys and liver. This may result in impaired functions.

Technology Process of Ethylbenzene

There total 1812 articles about Ethylbenzene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

: 104-55-2
3-phenyl-propenal

: 100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene

Guidance literature:: With palladium doped Hydrotalcite; In ethanol; at 150 ℃; for 2h; Microwave irradiation;
DOI:10.1002/cssc.201901934

Reference yield: 98.0%

: 98-85-1,13323-81-4
1-Phenylethanol

: 100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene

Guidance literature:: With C₂₁H₂₉ClIrN₄O₂⁽¹⁺⁾*CF₃O₃S^(1-); In 1,2-dichloro-benzene; at 150 ℃; for 4h; Reagent/catalyst; Inert atmosphere;
DOI:10.1016/j.jorganchem.2020.121290

Reference yield: 98.0%

: 100-52-7
benzaldehyde

: 100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene

Guidance literature:: With MoO₂Cl₂+(CH₃)3Al; In tetrahydrofuran; at -70 - 20 ℃; for 18h; Product distribution; further aldehydes and ketones, temperatures, various carbonyl-methylenating organomolybdenum aluminium and organotungsten aluminium complexes; also with Tebbe reagent;