Orlistat USP Related Compound C (Triphenylphosphine Oxide)
Product Information
Molecular Formula
C18H15OP
Molecular Weight
278.29
Description
Orlistat USP Related Compound C (Triphenylphosphine Oxide) is a pivotal compound in the realm of biochemical research, primarily recognized for its role as a byproduct in various chemical reactions. It is often utilized in the synthesis of complex organic molecules, serving as a catalyst or reagent due to its stable phosphine oxide structure. This compound's unique properties make it an essential component in laboratory settings, where precision and reliability are paramount. Its presence in research environments underscores its importance in advancing scientific understanding and innovation.
Synonyms
Triphenylphosphine Oxide; Triphenylphosphine Monoxide; Orlistat Related Compound C; Orlistat USP Related Compound C;
IUPAC Name
diphenylphosphorylbenzene
SMILES
C1=CC=C(C=C1)P(=O)(C2=CC=CC=C2)C3=CC=CC=C3
InChI
InChI=1S/C18H15OP/c19-20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
InChI Key
FIQMHBFVRAXMOP-UHFFFAOYSA-N
Boiling Point
360 °C
Melting Point
152-160 °C
Flash Point
356.0 °F - closed cup
Purity
≥ 99.5% (Assay)
Density
1,212 g/cm3
Solubility
Soluble in Chloroform, Ethyl Acetate, Methanol
Appearance
White crystal powder
Application
Used for processing (extraction, separation, and spectrophotometric determination) environmental samples of cadmium and mercury.
Storage
Store at RT
Safety Information
Hazards
H302 - H315 - H319 - H335
Precautionary Statement
P261 - P305 + P351 + P338
Computed Properties
XLogP3
2.8
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
3
Exact Mass
278.086052095 g/mol
Monoisotopic Mass
278.086052095 g/mol
Topological Polar Surface Area
17.1Ų
Heavy Atom Count
20
Formal Charge
0
Complexity
281
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-113999372-A | Phosphorus-containing super-crosslinked porous organic polymer material and preparation method and application thereof | 2021-12-21 |
| JP-2022040133-A | A photosensitive coloring composition for a color filter for a solid-state image sensor, a color filter, and a solid-state image sensor using the same. | 2021-12-15 |
| CN-114163621-A | Preparation method and application of epoxidized soybean oil and glycolide copolymerization bio-based elastomer | 2021-12-08 |
| CN-113880724-A | Preparation method of 3- (2-aminophenyl) -2-acrylate | 2021-12-06 |
| CN-114130791-A | Harmless treatment system for solid waste triphenylphosphine oxide in electronic industry | 2021-12-02 |
| CN-114057558-A | Synthetic method, catalytic system and application of 3,5, 5-trimethylhexanal | 2021-12-01 |
| CN-113860317-A | Method for producing silicon dioxide by synthesis method | 2021-11-24 |
| CN-114100541-A | Method for synthesizing isononanal by microchannel reaction device | 2021-11-23 |
| CN-114014859-A | Triazole indolol compound and synthesis method thereof | 2021-11-22 |
| CN-114031918-A | Polycarbonate composition with low yellowness index, and preparation method and application thereof | 2021-11-22 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 27725436 | 2016-01-01 | Ligand Activity of Group 15 Compounds Possessing Triphenyl Substituent for the RXR and PPARγ Nuclear Receptors | Biological & pharmaceutical bulletin |
| 25787141 | 2015-06-01 | Deoxynivalenol (Vomitoxin)-Induced Cholecystokinin and Glucagon-Like Peptide-1 Release in the STC-1 Enteroendocrine Cell Model Is Mediated by Calcium-Sensing Receptor and Transient Receptor Potential Ankyrin-1 Channel | Toxicological sciences : an official journal of the Society of Toxicology |
| 23022238 | 2012-11-02 | Gas chromatographic determination of phosphate-based flame retardants in styrene-based polymers from waste electrical and electronic equipment | Journal of chromatography. A |
| 22757962 | 2012-07-16 | Varying the Lewis base coordination of the Y2N2 core in the reduced dinitrogen complexes {[(Me3Si)2N]2(L)Y}2(μ-η2:η2-N2) (L = benzonitrile, pyridines, triphenylphosphine oxide, and trimethylamine N-oxide) | Inorganic chemistry |
| 22670799 | 2012-06-20 | A direct route to bis(imido)uranium(V) halides via metathesis of uranium tetrachloride | Journal of the American Chemical Society |
| 21847610 | 2012-06-01 | A convenient route to optically pure α-alkyl-β-(sec-amino)alanines | Amino acids |
| 22146808 | 2012-04-21 | Establishing the mechanism of Rh-catalysed activation of O2 by H2 | Dalton transactions (Cambridge, England : 2003) |
| 22589958 | 2012-04-01 | 7-Benzyl-3-(4-fluoro-phen-yl)-2-propyl-amino-5,6,7,8-tetra-hydro-pyrido[4',3':4,5]thieno[2,3-d]pyrimidin-4(3H)-one | Acta crystallographica. Section E, Structure reports online |
| 22412686 | 2012-03-01 | 7-Benzyl-3-(4-chloro-phen-yl)-2-isobutyl-amino-5,6,7,8-tetra-hydro-pyrido[4',3':4,5]thieno[2,3-d]pyrimidin-4(3H)-one | Acta crystallographica. Section E, Structure reports online |
| 22094964 | 2012-02-27 | The influence of reversible trianionic pincer OCO(3-)μ-oxo Cr(IV) dimer formation ([Cr(IV)]2(μ-O)) and donor ligands in oxygen-atom-transfer (OAT) | Dalton transactions (Cambridge, England : 2003) |
