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Bis(3-nitrophenyl)phosphinic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18593-20-9

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18593-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18593-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,9 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18593-20:
(7*1)+(6*8)+(5*5)+(4*9)+(3*3)+(2*2)+(1*0)=129
129 % 10 = 9
So 18593-20-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H9N2O6P/c15-13(16)9-3-1-5-11(7-9)21(19,20)12-6-2-4-10(8-12)14(17)18/h1-8H,(H,19,20)

18593-20-9Relevant academic research and scientific papers

Bridge-Caging Strategy in Phosphorus-Substituted Rhodamine for Modular Development of Near-Infrared Fluorescent Probes

Chai, Xiaoyun,Xiao, Jin,Li, Min,Wang, Chaoming,An, Haiyan,Li, Chen,Li, Yuntao,Zhang, Dazhi,Cui, Xiaoyan,Wang, Ting

, p. 14506 - 14512 (2018)

Replacement of the bridging oxygen atom in rhodamine with phosphorus is one of the most efficient ways for bright near-infrared (NIR) fluorophores with wavelengths over 700 nm. However, the organophosphorus bridge is more versatile than just being a spectrum tuner, it is also a profound solubility booster and photostability enhancer, as proved by a series of phosphorus-substituted rhodamines (PRBs). A unique bridge-caging strategy for efficiently manipulating fluorescence has further been innovated in example PRB2. Consistent with theoretical calculations, the formation of organophosphinate by a caging group as a fluorescence-controller locks the spirolactone into a colorless and nonfluorescent form, whereas decaging, a process induced by a specific stimulus, results in a ring-opened form, which yields strong fluorescence. The bridge-caging strategy is feasible for the modular development of NIR probes. Efficient in vivo imaging of photoillumination, hydrogen peroxide, and enzyme have been achieved on the PRB2 scaffold as a photoactivatable fluorophore, PRB2-hν; fluorescent indicator, PRB2-H2O2; and fluorogenic enzyme substrate, PRB2-NTR, respectively.

Bismuth Phosphinates in Bi-Nanocellulose Composites and their Efficacy towards Multi-Drug Resistant Bacteria

Werrett, Melissa V.,Herdman, Megan E.,Brammananth, Rajini,Garusinghe, Uthpala,Batchelor, Warren,Crellin, Paul K.,Coppel, Ross L.,Andrews, Philip C.

, p. 12938 - 12949 (2018)

A series of poorly soluble phenyl bis-phosphinato bismuth(III) complexes [BiPh(OP(=O)R1R2)2] (R1=R2=Ph; R1=R2=p-OMePh; R1=R2=m-NO2Ph; R1=Ph, R2=H; R1=R2=Me) have been synthesised and characterised, and shown to have effective antibacterial activity against Escherichia coli (E. coli), Staphylococcus aureus (S. aureus), methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE). The bismuth complexes were incorporated into microfibrillated (nano-) cellulose generating a bismuth-cellulose composite as paper sheets. Antibacterial evaluation indicates that the Bi-cellulose materials have analogous or greater activity against Gram positive bacteria when compared with commercial silver based additives: silver sulfadiazine loaded at 0.43 wt % into nanocellulose produces a 10 mm zone of inhibition on the surface of agar plates containing S. aureus whereas [BiPh(OP(=O)Ph2)2] loaded at 0.34 wt % produces an 18 mm zone of inhibition. These phenyl bis-phosphinato bismuth(III) complexes show potential to be applied in materials in healthcare facilities, to inhibit the growth of bacteria capable of causing serious disease.

ANTIBACTERIAL BISMUTH COMPLEXES

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Page/Page column 29, (2016/12/22)

Provided herein are organobismuth (III) phosphinate complexes, which comprise a phosphinate group and an aromatic carbocyclyl or aromatic heterocyclyl group. The complexes find use as antibacterial agents, and accordingly also provided herein are products

STUDY OF THE ALKALINE CLEAVAGE OF THE P-C BOND IN PHOSPHINE OXIDES AND DERIVATIVES OF TRICHLOROMETHANEPHOSPHONATE

Aksnes, Gunnar,Gierstae, Roald,Wulvik, Erik A.

, p. 141 - 152 (2007/10/02)

A study of alkaline decomposition of aromatic phosphine oxides containing p- and o-nitrobenzyl, and trichloromethyl as leaving groups, is reported.The property of the trichloromethyl group as leaving group, and the CCl3--group's further decomposition in the hydrolysis of diethyl and disodium trichloromethanephosphonates, have also been investigated.

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