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Phosphine oxide, (bromomethyl)diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119460-28-5

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119460-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119460-28-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,4,6 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 119460-28:
(8*1)+(7*1)+(6*9)+(5*4)+(4*6)+(3*0)+(2*2)+(1*8)=125
125 % 10 = 5
So 119460-28-5 is a valid CAS Registry Number.

119460-28-5SDS

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 [bromomethyl(phenyl)phosphoryl]benzene

1.2 Other means of identification

Product number -
Other names diphenylbromomethylphosphine 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:119460-28-5 SDS

119460-28-5Relevant academic research and scientific papers

C-2 auxiliaries for stereoselective glycosylation based on common additive functional groups

Boltje, Thomas J.,De Kleijne, Frank F. J.,Moons, Sam J.,White, Paul B.

, p. 1165 - 1184 (2020/02/22)

The stereoselective introduction of the glycosidic bond is one of the main challenges in chemical oligosaccharide synthesis. Stereoselective glycosylation can be achieved using neighbouring group participation of a C-2 auxiliary or using additives, for example. Both methods aim to generate a defined reactive intermediate that reacts in a stereoselective manner with alcohol nucleophiles. This inspired us to develop new C-2 auxiliaries based on commonly used additive functionalities such as ethers, phosphine oxides and tertiary amides. Good 1,2-trans-selectivity was observed for the phosphine oxide and amide-based auxiliaries expanding the toolbox with new auxiliaries for stereoselective glycosylation reactions.

C-Alkyl-bis-phosphoryl chelating systems for the potential recovery of strategic metals

Babouri, Rachida,Halidou Dougourikoye, Abdoul Razak,Ilagouma, Amadou TidJani,Pirat, Jean-Luc,Virieux, David,Volle, Jean-No?l

, (2020/09/07)

Methylene-bis-phosphonic acid and derivatives are used as complexing agents, diagnostics, therapeutics and show interesting virustatic properties. We describe the syntheses of mono- and di-substituted bisphosphonates and mono- and disubstituted diethyl ((diphenylphosphoryl)methyl)phosphonate as possible chelating systems for the recovery of strategic metals.

Ru-Ag and Ru-Au dicarbene complexes from an abnormal carbene ruthenium system

Bitzer, Mario J.,P?thig, Alexander,Jandl, Christian,Kühn, Fritz E.,Baratta, Walter

supporting information, p. 11686 - 11689 (2015/06/30)

Reaction of [Ru(OAc)2(PPh3)2] with a P-functionalized imidazolium bromide easily affords a cationic abnormal carbene Ru system. Metalation with Ag2O yields a Ru-Ag complex containing an anionic dicarbene ligand,

Synthesis and biological activity of dialkylamino-substituted phosphine oxides

Yarkevich,Petrova,Bachurin

, p. 1659 - 1664 (2013/02/23)

A series of dialkylamino-substituted phosphine oxides was synthesized and their physiological activity was studied. Pleiades Publishing, Ltd., 2012.

The effect of the phosphoryl group on the rate and mechanism of SN-substitution at the saturated carbon atoms

Tsvetkov, E. N.,Tkachenko, S. E.,Yarkevich, A. N.

, p. 339 - 341 (2007/10/02)

The reactivity of diarylphosphine oxides RR'P(O)CH2X with p-O2NC6H4ONa in DMF have been studied.The reaction rate increases with the electrodrawing properties of the substituents on R and R' in the following way: p-Me2NC6H4 2 reaction rate of diphenylphosphine oxides has been investigated.The reactivity increases as follows Cl I Br OTs.A reaction mechanism is suggested.

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