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2-(phenanthren-9-yl)cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73129-94-9

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73129-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73129-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,2 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 73129-94:
(7*7)+(6*3)+(5*1)+(4*2)+(3*9)+(2*9)+(1*4)=129
129 % 10 = 9
So 73129-94-9 is a valid CAS Registry Number.

73129-94-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenanthren-9-ylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2-(9-phenanthryl)cyclohexanone

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:73129-94-9 SDS

73129-94-9Relevant academic research and scientific papers

A three-step process to facilitate the annulation of polycyclic aromatic hydrocarbons

Martin, Sara E.,Streeter, Matthew D.,Jones, Laurel L.,Klepfer, Matthew S.,Atmatzidis, Kyriakos,Wille, Kristen D.,Harrison, Sean A.,Hoegg, Edward D.,Sheridan, Heather M.,Kramer, Stephanie,Parrish, Damon A.,Amick, Aaron W.

, p. 8324 - 8330 (2015/03/18)

A new efficient three-step process to annulate polycyclic aromatic hydrocarbons (PAHs) has been developed, providing access to PAHs with saturated rings that under current chemical methods would be difficult to produce in an efficient manner. This method relies on a palladium-catalyzed cross-coupling reaction of various brominated PAHs with cyclohexanone to yield α-arylated ketones, which are converted to regiospecific vinyl triflates and cyclized by a palladium-catalyzed intramolecular arene-vinyl triflate coupling to produce PAHs with incorporated saturated rings or "tetrahydroindeno-annulated" PAHs.

Policyclic Fluoranthene Hydrocarbons. 2. A New General Synthesis

Cho, Bongsup P.,Harvey, Ronald G.

, p. 5668 - 5678 (2007/10/02)

A novel and efficient synthetic approach to policyclic fluoranthene hydrocarbons is described.The method entails fusion of an indeno ring to an appropriate alternant hydrocarbon via reaction of its aryllithium derivative with cyclohexene oxide, followed by oxidation, cyclodehydration, and aromatization.Cyclization of the cyclohexanone and cyclohexanol derivatives of the policyclic aromatic ring systems studied proceeds with high regioselectivity, and the direction of ring closure is predictable by molecular orbital methods.This synthetic approach provides a convenient general route to polyaromatic fluoranthene compounds, including potentially carcinogenic members of this class.Hydrocarbons synthesized by this method include benzacephenanthrylene (1), indenopyrene (2), indenochrysene (3), benzindenochrysene (4), fluorenochrysene (5), dibenzaceanthrylene (6), dibenzaceanthrylene (7), benzaceanthrylene (8), benzindenochrysene (9), fluorenochrysene (10), and dibenzacephenanthrylene (11).

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