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2-methoxybenzo[c]phenanthrene is a polycyclic aromatic hydrocarbon (PAH) with a molecular formula of C21H16O. It is a derivative of benzo[c]phenanthrene, featuring a methoxy group (-OCH3) attached to the 2-position of the benzene ring. 2-methoxybenzo[c]phenanthrene is characterized by its complex, planar structure consisting of four fused benzene rings, with the methoxy group providing additional functionality. 2-methoxybenzo[c]phenanthrene is known for its potential environmental and health impacts, as PAHs are often found in polluted air, water, and soil, and some are classified as carcinogenic. The presence of the methoxy group may influence its reactivity, solubility, and toxicity compared to the parent compound. Due to its complex structure and potential health risks, research on 2-methoxybenzo[c]phenanth oftenrene focuses on understanding its environmental fate and effects on human health.

4176-45-8

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4176-45-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4176-45-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,7 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4176-45:
(6*4)+(5*1)+(4*7)+(3*6)+(2*4)+(1*5)=88
88 % 10 = 8
So 4176-45-8 is a valid CAS Registry Number.

4176-45-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxybenzo[c]phenanthrene

1.2 Other means of identification

Product number -
Other names 2-Methoxy-benzo<c>phenanthren

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4176-45-8 SDS

4176-45-8Relevant academic research and scientific papers

Synthesis of Helical Quinone Derivatives by Oxidative Coupling of Substituted 2-Hydroxybenzo[c]phenanthrenes

Shahabuddin, Mohammad,Akutsu, Akira,Kimura, Takao,Karikomi, Michinori

, p. 1547 - 1554 (2017/03/21)

A concise synthesis of novel substituted quinone derivatives from commercially available starting materials was developed. For this synthesis, classical photo-induced 6π-electrocyclization was utilized, followed by oxidative aromatization reaction, and su

Efficient Enantioselective Synthesis of Oxahelicenes Using Redox/Acid Cooperative Catalysts

Sako, Makoto,Takeuchi, Yoshiki,Tsujihara, Tetsuya,Kodera, Junpei,Kawano, Tomikazu,Takizawa, Shinobu,Sasai, Hiroaki

, p. 11481 - 11484 (2016/10/06)

An efficient and enantioselective synthesis of oxa[9]helicenes has been established via vanadium(V)-catalyzed oxidative coupling/intramolecular cyclization of polycyclic phenols. A newly developed vanadium complex cooperatively functions as both a redox and Lewis acid catalyst to promote the present sequential reaction and afford oxa[9]helicenes in good yields with up to 94% ee.

Continuous flow photocyclization of stilbenes-scalable synthesis of functionalized phenanthrenes and helicenes

Lefebvre, Quentin,Jentsch, Marc,Rueping, Magnus

supporting information, p. 1883 - 1890 (2013/10/22)

A continuous flow oxidative photocyclization of stilbene derivatives has been developed which allows the scalable synthesis of backbone functionalized phenanthrenes and helicenes of various sizes in good yields.

Palladium-catalyzed intramolecular C-H activation: A synthetic approach towards polycyclic aromatic hydrocarbons

Paul, Sunanda,Jana, Rathin,Ray, Jayanta K.

experimental part, p. 1463 - 1468 (2010/08/20)

A simple and convenient synthetic protocol for the construction of polycyclic aromatic hydrocarbons has been developed. A variety of phenanthrene, benzo[c]phenanthrene and chrysene derivatives was synthesized via Pd-catalyzed intramolecular C-H activation followed by acid-catalyzed water elimination.

Synthesis of derivatives of phenanthrene and helicene by improved procedures of photocyclization of stilbenes

Talele, Harish R.,Gohil, Monik J.,Bedekar, Ashutosh V.

experimental part, p. 1182 - 1186 (2009/12/25)

An improved method has been developed for photocyclization of stilbene to construct phenanthrenes and benzo[c]phenanthrenes. This reaction is promoted by iodine while tetrahydrofuran is used as an efficient and inexpensive scavenger of hydroiodic acid produced during the photocyclization sequence. In another process, cyclohexene is used as a reagent for dehydrogenation step in place of THFI2.

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