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1304574-81-9

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1304574-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1304574-81-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,4,5,7 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1304574-81:
(9*1)+(8*3)+(7*0)+(6*4)+(5*5)+(4*7)+(3*4)+(2*8)+(1*1)=139
139 % 10 = 9
So 1304574-81-9 is a valid CAS Registry Number.

1304574-81-9Relevant academic research and scientific papers

Self-reporting heavy atom-free photodynamic therapy agents

Demirok, Naime,Erbas-Cakmak, Sundus,Kayadibi Koygun, Gozde,Turkoglu, Gulsen,Yurt, Mediha Nur Zafer

supporting information, p. 9433 - 9437 (2020/12/15)

Two novel, self-reporting distyryl BODIPY-based photodynamic therapy agents functionalized with singlet oxygen responsive imidazole and tertiary amine moieties are developed. Heavy atom-free photosensitizers are demonstrated to have efficient photodynamic action in MCF7 cells. The fluorescence intensity of the photosensitizers is shown to be reduced as a result of 1O2 generation without any significant change in photodynamic activity. This journal is

Selective photosensitization through an and logic response: Optimization of the pH and glutathione response of activatable photosensitizers

Erbas-Cakmak, Sundus,Cakmak, Fatma Pir,Topel, Seda Demirel,Uyar, Taha Bilal,Akkaya, Engin U.

, p. 12258 - 12261 (2015/07/27)

A series of pH and GSH responsive photosensitizers were designed and synthesized. pKa values were optimized by adjusting the inductive contribution of substituents to reach a pH range (6.0-7.4) relevant to the tumour microenvironment. pH-Activatable behaviour and redox mediated release of the quencher from the PS by GSH allow the construction of an AND logic operator for selective photodynamic action in aqueous solutions.

BODIPY-based donor-acceptor π-conjugated alternating copolymers

Popere, Bhooshan C.,Della Pelle, Andrea M.,Thayumanavan

, p. 4767 - 4776 (2012/05/20)

Four novel π-conjugated copolymers incorporating 4,4-difluoro-4-borata- 3a-azonia-4a-aza-s-indacene (BODIPY) core as the "donor" and quinoxaline (Qx), 2,1,3-benzothiadiazole (BzT), N,N′-di(2′-ethyl) hexyl-3,4,7,8-naphthalenetetracarboxylic diimide (NDI), and N,N′- di(2′-ethyl)hexyl-3,4,9,10-perylene tetracarboxylic diimide (PDI) as acceptors were designed and synthesized via Sonogashira polymerization. The polymers were characterized by 1H NMR spectroscopy, gel permeation chromatography (GPC), UV-vis absorption spectroscopy, and cyclic voltammetry. Density functional theory (DFT) calculations were performed on polymer repeat units, and the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) energy levels were estimated from the optimized geometry using B3LYP functional and 6-311g(d,p) basis set. Copolymers with Qx and BzT possessed HOMO and LUMO energy levels comparable to those of BODIPY homopolymer, while PDI stabilized both HOMO and LUMO levels. Semiconductor behavior of these polymers was estimated in organic thin-film transistors (OTFT). While the homopolymer, Qx, and BzT-based copolymers showed only p-type semiconductor behavior, copolymers with PDI and NDI showed only n-type behavior.

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