604-49-9 Usage
Polycyclic aromatic hydrocarbon
Benzoquinoline structure
The compound is a polycyclic aromatic hydrocarbon, which means it consists of multiple aromatic rings fused together, in this case, forming a benzoquinoline structure.
Methyl group attachment
Benzene ring
A methyl group (CH3) is attached to one of the benzene rings in the 1-Methylbenzo[f]quinoline structure, contributing to its chemical properties.
Biological activity
Anti-tumor and anti-inflammatory properties
1-Methylbenzo[f]quinoline has been studied for its potential biological activity, including its ability to exhibit anti-tumor and anti-inflammatory effects.
Research applications
Organic chemistry and material science
The compound is used in research related to organic chemistry and material science, aiding in the development and understanding of new compounds and materials.
Synthesis
Pharmaceutical and agrochemical industries
1-Methylbenzo[f]quinoline is used as an intermediate or building block in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new products in these industries.
Precautions
Aromatic nature and potential health risks
Due to its aromatic nature and the potential health risks associated with exposure to polycyclic aromatic hydrocarbons, appropriate safety measures should be taken when handling and using 1-Methylbenzo[f]quinoline.
Check Digit Verification of cas no
The CAS Registry Mumber 604-49-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 604-49:
(5*6)+(4*0)+(3*4)+(2*4)+(1*9)=59
59 % 10 = 9
So 604-49-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H11N/c1-10-8-9-15-13-7-6-11-4-2-3-5-12(11)14(10)13/h2-9H,1H3