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2-phenylanthracen-9(10H)-one is an organic compound with the molecular formula C22H15NO. It is a derivative of anthracenone, featuring a phenyl group attached to the 2-position of the anthracene core. 2-phenylanthracen-9(10H)-one is characterized by its tricyclic structure, with the anthracene ring system and the phenyl ring connected through a carbon-carbon bond. It is a white crystalline solid and is often used in the synthesis of various organic compounds and pharmaceuticals due to its unique structure and reactivity. The compound's properties, such as its melting point, solubility, and stability, can be influenced by the presence of the phenyl group, making it a valuable building block in organic chemistry.

1714-13-2

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1714-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1714-13-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,1 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1714-13:
(6*1)+(5*7)+(4*1)+(3*4)+(2*1)+(1*3)=62
62 % 10 = 2
So 1714-13-2 is a valid CAS Registry Number.

1714-13-2SDS

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 2-phenyl-10H-anthracen-9-one

1.2 Other means of identification

Product number -
Other names 9-Oxo-2-phenyl-9.10-dihydro-anthracen

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

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More Details:1714-13-2 SDS

1714-13-2Relevant academic research and scientific papers

Synthesis of Annulated Anthracenes, Carbazoles, and Thiophenes Involving Bradsher-Type Cyclodehydration or Cyclization-Reductive-Dehydration Reactions

Rafiq, Settu Muhamad,Sivasakthikumaran, Ramakrishnan,Karunakaran, Jayachandran,Mohanakrishnan, Arasambattu K.

, p. 5099 - 5114 (2015/08/18)

A conventional BF3·OEt2-mediated Bradsher-type cyclodehydration of 2-arylmethyl benzaldehydes in CH2Cl2 at room temperature gave polycyclic aromatic and heteroaromatic compounds. Alternatively, these compounds could be synthesized in better yields from 2-arylmethylbenzoic acids by triflic-acid-mediated cyclization followed by reductive dehydration.

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