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1H-Phosphole, 2,5-dihydro-1,3,4-triphenyl-, 1-oxide is a complex organic compound with the chemical formula C24H19OP. It is a derivative of phosphole, a heterocyclic compound containing a phosphorus atom in a five-membered ring. The molecule features three phenyl groups attached to the phosphole ring at positions 1, 3, and 4, and a hydroxyl group at the 2-position. The 1-oxide designation indicates the presence of an oxygen atom bonded to the phosphorus atom, forming a phosphorus oxide. 1H-Phosphole, 2,5-dihydro-1,3,4-triphenyl-, 1-oxide is of interest in organic chemistry and materials science due to its unique electronic properties and potential applications in the development of new materials and pharmaceuticals.

55781-96-9

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55781-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55781-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,8 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55781-96:
(7*5)+(6*5)+(5*7)+(4*8)+(3*1)+(2*9)+(1*6)=159
159 % 10 = 9
So 55781-96-9 is a valid CAS Registry Number.

55781-96-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,4-triphenyl-2,5-dihydro-1λ<sup>5</sup>-phosphole 1-oxide

1.2 Other means of identification

Product number -
Other names 1H-Phosphole,2,5-dihydro-1,3,4-triphenyl-,1-oxide

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:55781-96-9 SDS

55781-96-9Relevant academic research and scientific papers

The synthesis of stable 1,3,4-triphenylphospholes

Niemi, Tuula-A.,Coe, Paul L.,Till, Stephen J.

, p. 1519 - 1528 (2007/10/03)

The first syntheses of 1,3,4-triphenylphosphole, 2-bromo-l,3,4-phenylphosphole and 2,5-dibromo-l,3,4-triphenylphosphole are described. These phospholes, unlike most of the known derivatives, are difficult to oxidise and they and their corresponding oxides show little tendency to dimerise. The NBS mediated bromination of 1,3,4-triphenyl2,5-dihydrophosphole oxide led to the desired precursors of the corresponding phospholes and in one case unexpectedly yielded a phosphole oxide directly. Some reactions including the formation of organolithium reagents and their derivatisation are reported. McMurry reactions of derived formylphospholes to give coupled products are described and some copper mediated reactions are also discussed. The Royal Society of Chemistry 2000.

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