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sodium tris(4-methylphenyl)(phenyl)borate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54873-16-4

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54873-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54873-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,7 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54873-16:
(7*5)+(6*4)+(5*8)+(4*7)+(3*3)+(2*1)+(1*6)=144
144 % 10 = 4
So 54873-16-4 is a valid CAS Registry Number.

54873-16-4Downstream Products

54873-16-4Relevant academic research and scientific papers

COMPOUNDS AND METHODS FOR THE TREATMENT OF PATHOGENIC NEISSERIA

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Page/Page column 41, (2020/05/06)

Tetracoordinate organoborate compounds, such as compounds harboring a tetraarylborate anion or a triarylalkylborate anion, are shown to exhibit a selective bacteriostatic and bactericidal effect against pathogenic Neisseria species such as N. meningitidis

Reaction of organoboron compounds with platinum(II) disolvento complexes

Siegmann, Konstantin,Pregosin, Paul S.,Venanzi, Luigi M.

, p. 2659 - 2664 (2008/10/08)

Cationic complexes cis-[Pt(S)2L2]2+ (L = PMe3, PEt3, or PPh3; S = H2O or MeOH) react with arylboron derivatives ([BPh4]-, [B(p-Tol)4]-, [B(m-Tol)4]-, BPh3, B(OMe)Ph2, B(OMe)2Ph, and B(OH)2Ph) to give trans-[Pt(Ar)(S)L2]+ which are isolated and characterized as their halo derivatives trans-[PtX(Ar)L2]. When L = PMe3, the transient formation of cis-[Pt(Ar)(S)L2]+ is also observed. The cation cis-[Pt(CH3CN)2-(PEt3)2] 2+, however, reacts with [BPh4]- only when at least some of the solvent is hydroxylic. However the phenylation and cis-trans isomerization reactions are slowed down so that the intermediate formation of cis-[Pt(Ph)(CH3CN)(PEt3)2]+ cation can be observed. It is shown that [BPh4]- is not the phenylating agent as it decomposes to BPh3 and C6H6 prior to the phenylation reaction. Other phenylboron derivatives such as BPh3, B(OMe)Ph2, B(OMe)2Ph, and B(OH)2Ph can transfer all of their phenyl groups to platinum. It is found that the phenyl transfer is strictly regioselective; i.e., only the C atom bonded to boron is found coordinated to platinum. When [B(Me)(Ph)3]- is used, either a methyl or a phenyl group can be transferred to platinum.

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