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Phenanthridine, 6-(diphenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52648-59-6

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52648-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52648-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,4 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52648-59:
(7*5)+(6*2)+(5*6)+(4*4)+(3*8)+(2*5)+(1*9)=136
136 % 10 = 6
So 52648-59-6 is a valid CAS Registry Number.

52648-59-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-diphenylmethylphenanthridine

1.2 Other means of identification

Product number -
Other names 6-benzhydryl-phenanthridine

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:52648-59-6 SDS

52648-59-6Downstream Products

52648-59-6Relevant academic research and scientific papers

Rapid synthesis of polysubstituted phenanthridines from simple aliphatic/aromatic nitriles and iodo arenes: Via Pd(ii) catalyzed domino C-C/C-C/C-N bond formation

Jaiswal, Yogesh,Kumar, Yogesh,Pal, Jagannath,Subramanian, Ranga,Kumar, Amit

supporting information, p. 7207 - 7210 (2018/07/03)

An efficient and straightforward method has been developed for the synthesis of polysubstituted phenanthridines from simple aryl iodides and alkyl/aryl nitriles via the palladium-catalyzed nucleophilic addition of aryl iodides to nitriles followed by casc

Medium and Substituent Effects on the Photochemistry of Phenanthridine N-Oxides. Is an Intermediate of Diradical Character involved in the Photorearrangement of Heterocyclic N-Oxides?

Albini, Angelo,Fasani, Elisa,Frattini, Valeria

, p. 235 - 240 (2007/10/02)

The photochemistry of several 6-substituted phenanthridine N-oxides has been investigated, or reinvestigated, in benzene and ethanol.The main processes observed are: (a) 1,2-oxygen and substituent shift to yield N-substituted phenanthridones (2) and (b) ring enlargements to dibenzo-1,3-oxazepines (7).With 6-diphenylmethylphenanthridine N-oxide (1b) rearrangement (a) predominates and occurs with 45percent substituent loss in benzene (but only 2percent in ethanol).With the 6-phenylderivative (1c) process (a) predominates in ethanol and process (b) in benzene and with the 6-p-nitrophenyl derivative (1d) the latter process predominates in both solvents.With 6-cyanophenanthridine N-oxide (1e) rearrangement (b) predominates in benzene; in the presence of 2,3-dimethylbutene (but not of cyclohexene) addition products are obtained; with dienes deoxygenation is the main process.Medium and substituents may change the nature of the lowest excited singlet state, but more importantly affect the stability of an intermediate of diradical character occurring along the reaction pathway, thus driving it towards rearrangement (a) or (b).Intermediate diradicals are unambiguously indicated only in particular cases but their role is probably more general.

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