Benzene, ethenyl-, trimer

Base Information

Chemical Name:Benzene, ethenyl-, trimer
CAS No.:28213-80-1
Deprecated CAS:1401716-44-6
Molecular Formula:C8H10
Molecular Weight:106.17
Hs Code.:
European Community (EC) Number:208-645-1
NSC Number:4957
UNII:239WSR2IBO
DSSTox Substance ID:DTXSID1060211
Nikkaji Number:J24.280B,J2.700.985I
Wikipedia:Phenylacetylene
Wikidata:Q417321
ChEMBL ID:CHEMBL234833

Synonyms:Benzene, ethenyl-, trimer;STYRENE TRIMERS;

Suppliers and Price of Benzene, ethenyl-, trimer

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 22 raw suppliers

Chemical Property of Benzene, ethenyl-, trimer

Chemical Property:

Boiling Point:136.2°Cat760mmHg
Flash Point:25.9°C
Density:0.868g/cm³
XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:102.0469501914
Heavy Atom Count:8
Complexity:98.5

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Chemical Classes:Other Classes -> Aromatic Hydrocarbons
Canonical SMILES:C#CC1=CC=CC=C1

Technology Process of Benzene, ethenyl-, trimer

There total 1815 articles about Benzene, ethenyl-, trimer 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;