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1-methoxybenzo[c]phenanthrene is a polycyclic aromatic hydrocarbon (PAH) consisting of a benzo[c]phenanthrene core with a methoxy group attached at the 1-position. It is a complex organic molecule with a fused ring structure, characterized by the presence of multiple benzene rings. 1-methoxybenzo[c]phenanthrene is of interest in the field of organic chemistry and environmental science, as PAHs are known to be carcinogenic and can be released into the environment through various industrial processes and combustion of organic materials. The methoxy group in 1-methoxybenzo[c]phenanthrene contributes to its unique chemical properties, making it a subject of study for potential applications and understanding its environmental impact.

4235-05-6

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4235-05-6 Usage

Type

Polycyclic aromatic hydrocarbon (PAH) compound

Origin

Derived from the combustion of organic materials such as coal, oil, and gas

Physical form

Colorless, crystalline solid

Molecular weight

250.31 g/mol

Carcinogenicity

Classified as a potential human carcinogen by the International Agency for Research on Cancer (IARC)

Health risks

Known to pose serious health risks if inhaled or ingested, exposure has been linked to respiratory and cardiovascular diseases, and an increased risk of cancer (particularly lung cancer)

Regulations

Strict guidelines in place to limit human exposure in occupational and environmental settings.

Check Digit Verification of cas no

The CAS Registry Mumber 4235-05-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,3 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4235-05:
(6*4)+(5*2)+(4*3)+(3*5)+(2*0)+(1*5)=66
66 % 10 = 6
So 4235-05-6 is a valid CAS Registry Number.

4235-05-6Upstream product

4235-05-6Downstream Products

4235-05-6Relevant academic research and scientific papers

Synthesis of 1-(2-ethynyl-6-methylphenyl)- and 1-(2-ethynyl-6-methoxyphenyl)-naphthalene and their cyclization

Storch, Jan,?ermák, Jan,Karban, Jind?ich

, p. 6814 - 6816 (2008/03/12)

A Suzuki cross-coupling reaction of hindered 2-bromo-1-trimethylsilylethynylbenzenes with 1-naphthaleneboronic acid yielding (2-ethynylphenyl)naphthalenes has been achieved. Their subsequent cyclization was carried out, giving benzo[c]phenanthrenes, without the use of photochemical procedures.

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