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(3-Hydroxypropyl)-phenylphosphan, also known as 3-(phenylphosphanyl)propan-1-ol, is an organophosphorus compound characterized by a phosphorus atom bonded to a phenyl group and a 3-hydroxypropyl group. (3-Hydroxypropyl)-phenylphosphan is a colorless liquid with a molecular formula of C9H13O2P and a molecular weight of 182.17 g/mol. It is used in various applications, including as a flame retardant, a stabilizing agent for plastics, and in the synthesis of other organophosphorus compounds. Due to its phosphorus content, it can also be used in the production of pesticides and as a precursor in the pharmaceutical industry. The compound is sensitive to moisture and should be stored under dry conditions to prevent hydrolysis.

2468-10-2

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2468-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2468-10-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,6 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2468-10:
(6*2)+(5*4)+(4*6)+(3*8)+(2*1)+(1*0)=82
82 % 10 = 2
So 2468-10-2 is a valid CAS Registry Number.

2468-10-2Downstream Products

2468-10-2Relevant academic research and scientific papers

CsOH-promoted epoxide ring-opening with phosphines: Mild and efficient synthesis of monohydroxyphosphines

Fox, Daniel L.,Robinson, Ashlee A.,Frank, James B.,Salvatore, Ralph Nicholas

, p. 7579 - 7582 (2003)

A mild and convenient synthesis of monohydroxyphosphines has been achieved by epoxide ring-opening using primary or secondary phosphines in the presence of cesium hydroxide, 4 ? molecular sieves and DMF at room temperature. These reaction conditions were

A Simple Synthesis and Some Synthetic Applications of Substituted Phosphide and Phosphinite Anions

Tsvetkov, E. N.,Bondarenko, N. A.,Malakhova, I. G.,Kabachnik, M. I.

, p. 198 - 208 (2007/10/02)

Based on data for the acidity relationship of phosphines and phosphinous acids and water in dimethyl sulfoxide and water, a simple method is reported for the generation of phosphide and phosphinite anions by the action of concentrated aqueous alkali on primary and secondary phosphines as well as phosphinous acids in dimethyl sulfoxide or other dipolar aprotic solvents.Alkylation of the anion yields secondary and tertiary phosphines, polyphosphines, functionally substituted phosphines as well as similarly substituted phosphine oxides.Phosphinous acids have beenalkylated in various solvents in two-phase systems containing concentrated aqueous alkali and tetrabutylammonium iodide as phase transfer catalyst.

Carbonic Ester Phosphides - Synthesis and Cyclization Reactions

Thamm, Ruediger,Fluck, Ekkehard

, p. 965 - 974 (2007/10/02)

Carbonic ester phosphides, RPHCOOR' and RP(COOR')2, have been prepared by the reaction of ClCOOR' with primary phosphines RPH2 in the presence of K2CO3.Some compounds of RPHCOOR' series are transformed into P-heterocycles through addition of the P-H group to the C=C doublebond systems.The 31P NMR data, IR and mass spectra of the novel compounds are presented and discussed. - Keywords: Carbonic Ester Phosphides, Mass Spectra, IR Spectra, NMR Spectra

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