6366-24-1 Usage
Chemical Family
Polycyclic Aromatic Hydrocarbons (PAHs)
Type
Chlorinated derivative of 7-methylbenz[a]anthracene
Environmental Impact
Known environmental pollutant
Health Risk
Carcinogenic and hazardous to human health
Mutagenic Properties
Potent mutagen
DNA Interaction
Induces DNA damage
Safety Measures
Minimize exposure and use appropriate safety measures when handling
Chemical Structure
Contains a chlorine atom at the 10th position and a methyl group at the 7th position on the benz[a]anthracene molecule
Physical Properties
Likely to be a solid at room temperature, with a high melting point and low solubility in water
Chemical Reactivity
May react with nucleophilic reagents, such as amines or thiols, due to the presence of the chlorine atom.
Check Digit Verification of cas no
The CAS Registry Mumber 6366-24-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6366-24:
(6*6)+(5*3)+(4*6)+(3*6)+(2*2)+(1*4)=101
101 % 10 = 1
So 6366-24-1 is a valid CAS Registry Number.
InChI:InChI=1/C19H13Cl/c1-12-16-9-7-15(20)10-14(16)11-19-17(12)8-6-13-4-2-3-5-18(13)19/h2-11H,1H3
6366-24-1Relevant articles and documents
Aldimine-directed branched-selective hydroarylation of styrenes
Lee, Pin-Sheng,Yoshikai, Naohiko
, p. 1240 - 1244 (2013/03/13)
Branching out: A simple and inexpensive cobalt/triarylphosphine catalyst promotes aldimine-directed hydroarylation of styrene with high branched regioselectivity to afford 1,1-diarylethane derivatives in good yields under mild reaction conditions. The ortho-formyl group in the hydroarylation products is amenable to dehydrative cyclization, to give fused polycyclic aromatic hydrocarbons, as well as decarbonylative removal. Copyright
