1-Chloroanthracene

Base Information

• Chemical Name: 1-Chloroanthracene
• CAS No.: 4985-70-0
• Molecular Formula: C14H9 Cl
• Molecular Weight: 212.678
• European Community (EC) Number: 225-641-5
• NSC Number: 4218
• DSSTox Substance ID: DTXSID40871110
• Nikkaji Number: J3.069D
• Wikidata: Q81986593
• Mol file: 4985-70-0.mol

Synonyms:1-Chloroanthracene;4985-70-0;Anthracene, 1-chloro-;CHLOROANTHRACENE;1-chloro-anthracene;CCRIS 5548;NSC 4218;EINECS 225-641-5;50602-11-4;NSC4218;Anthracene, chloro-;1-Chloroanthracene, 95%;SCHEMBL476842;Anthracene, 1-chloro- (8CI);SRIHSAFSOOUEGL-UHFFFAOYSA-;DTXSID40871110;NSC-4218;AKOS030573760;LS-188340;FT-0635499

Chemical Property of 1-Chloroanthracene

Chemical Property:

• Vapor Pressure: 2.42E-05mmHg at 25°C
• Melting Point: 77-80 °C(lit.)
• Refractive Index: 1.6959
• Boiling Point: 370.1°Cat760mmHg
• Flash Point: 179.2°C
• PSA: 0.00000
• Density: 1.253g/cm³
• LogP: 4.64640
• XLogP3: 5.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 212.0392780
• Heavy Atom Count: 15
• Complexity: 225

Purity/Quality:

97% ^*data from raw suppliers

1-Chloroanthracene 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Other Classes -> Polycyclic Aromatic Hydrocarbons
• Canonical SMILES: C1=CC=C2C=C3C(=CC2=C1)C=CC=C3Cl
• Description: 1-Chloroanthracene forms photodimer trans-bi(1-chloro-9,10-dihydro-9,10-anthracenediyl) via the solid-state [4+4]-photodimerization.1-Chloroanthracene was used to investigate the effect of polycyclic aromatic hydrocarbons on gap junctional intercellular communication and activation of intracellular receptor kinase in F344 rat liver epithelial cells.
• Uses: 1-Chloroanthracene was used to investigate the effect of polycyclic aromatic hydrocarbons on gap junctional intercellular communication and activation of intracellular receptor kinase in F344 rat liver epithelial cells.

Technology Process of 1-Chloroanthracene

There total 9 articles about 1-Chloroanthracene 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: 88.0%

1-chloroanthracene-9,10-dione (82-44-0) → 1-chloroanthracene (4985-70-0)

Guidance literature:

With sodium hydroxide; zinc; for 18h; Heating;

Reference yield: 85.0%

4-chloroanthrone (4888-02-2) → 1-chloroanthracene (4985-70-0)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; for 0.25h;

DOI:10.1021/jo00360a054

Reference yield: 20.0%

N-(4-Chloro-anthracen-9-yl)-formamide (79917-76-3) → 1-chloroanthracene (4985-70-0)

Guidance literature:

With formic acid; formamide; for 9h; Heating;

DOI:10.1021/jo00341a047

upstream raw materials:

tetrachloromethane

1-chloroanthracene-9,10-dione

4-chloroanthrone

N-(4-Chloro-anthracen-9-yl)-formamide

Downstream raw materials:

1-hydroxyanthracene

anthracene-1-carbonitrile

8,10-dichloroanthracene

1-chlorotriptycene