8-Methylbenz[a]anthracene

Base Information

Chemical Name:8-Methylbenz[a]anthracene
CAS No.:2381-31-9
Molecular Formula:C19H14
Molecular Weight:242.32
Hs Code.:2902909090
European Community (EC) Number:661-768-6
NSC Number:409458
UNII:LP9SKC568Q
DSSTox Substance ID:DTXSID10178522
Nikkaji Number:J35.567D
Wikidata:Q27283108
Mol file:2381-31-9.mol

Synonyms:8-methylbenz(a)anthracene;8-methylbenzanthracene

Suppliers and Price of 8-Methylbenz[a]anthracene

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

TRC
8-Methylbenz[a]anthracene
100mg
$ 1320.00

Medical Isotopes, Inc.
8-Methylbenz[a]anthracene
100 mg
$ 2200.00

American Custom Chemicals Corporation
8-METHYLBENZ[A]ANTHRACENE 95.00%
5MG
$ 504.42

Total 9 raw suppliers

Chemical Property of 8-Methylbenz[a]anthracene

Chemical Property:

Vapor Pressure:7.61E-08mmHg at 25°C
Melting Point:156.5°C
Refractive Index:1.7480 (estimate)
Boiling Point:449.4°Cat760mmHg
Flash Point:217.8°C
PSA：0.00000
Density:1.164g/cm³
LogP:5.45460
XLogP3:6.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:242.109550447
Heavy Atom Count:19
Complexity:320

Purity/Quality:

99% ^*data from raw suppliers

8-Methylbenz[a]anthracene ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Other Classes -> Polycyclic Aromatic Hydrocarbons
Canonical SMILES:CC1=C2C=C3C=CC4=CC=CC=C4C3=CC2=CC=C1
Uses 8-Methylbenz[a]anthracene is a monomethylated polycyclic aromatic hydrocarbon with carcinogenic activity.

Technology Process of 8-Methylbenz[a]anthracene

There total 1 articles about 8-Methylbenz[a]anthracene 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: