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16,17-Dihydro-15H-cyclopenta[a]phenanthrene is a polycyclic aromatic hydrocarbon (PAH) with the molecular formula C20H16. It is a derivative of cyclopenta[a]phenanthrene, which is a type of PAH consisting of five fused benzene rings. The compound is characterized by the presence of a cyclopentane ring fused to the phenanthrene structure, and the dihydro prefix indicates that it has two hydrogen atoms added to the parent compound. This chemical is known for its potential environmental and health impacts, as many PAHs are carcinogenic and can be released into the environment through various industrial processes and combustion of organic materials. Due to its complex structure and potential risks, research on 16,17-Dihydro-15H-cyclopenta[a]phenanthrene often focuses on understanding its formation, behavior in the environment, and methods for its detection and mitigation.

482-66-6

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482-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 482-66-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 482-66:
(5*4)+(4*8)+(3*2)+(2*6)+(1*6)=76
76 % 10 = 6
So 482-66-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H14/c1-2-6-14-12(4-1)8-10-17-15-7-3-5-13(15)9-11-16(14)17/h1-2,4,6,8-11H,3,5,7H2

482-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 16,17-dihydro-15H-cyclopenta[a]phenanthrene

1.2 Other means of identification

Product number -
Other names dihydrocyclopenta<a>phenanthrene

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:482-66-6 SDS

482-66-6Relevant academic research and scientific papers

Acid-catalyzed rearrangement of cyclobutanols. Syntheses of chrysenes, cyclopentenophenanthrenes, and diarylmethanes

Lee-Ruff, Edward,Hopkinson, Alan C.,Kazarians-Moghaddam, Hira,Gupta, Brij,Katz, Morris

, p. 154 - 159 (2007/10/02)

Acid-catalyzed reactions of 8-aryl or 8,8-diarylbicyclooct-2-en-7-ols lead to tetrahydrophenanthrene derivatives.For example 8-(1-naphthyl)-bicyclooct-2-en-7-ols give substituted chrysenes in methanesulphonic acid.In the case of the homologous 7-aryl or 7,7-diarylbicyclohept-2-en-6-ols a novel transformation of diarylmethanes is observed.A mechanism is proposed which accounts for the product distribution observed in these rearrangements.

A NOVEL ACID-CATALYZED REARRANGEMENT OF CYCLOBUTANOLS

Lee-Ruff, Edward,Hopkinson, Alan C.,Kazarians-Moghaddam, Hira,Duperrouzel, Paul,Gupta, Brij,Katz, Morris

, p. 4917 - 4920 (2007/10/02)

Under acid-catalysis 7-arylbicyclohept-2-en-6-ols rearrange to diarylmethanes and cyclopenteno-annelated polycyclic aromatic hydrocarbons

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