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Benzenamine, 3,3'-diselenobis[N,N-diethyl-4-nitroso- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

910540-74-8

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910540-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 910540-74-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,5,4 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 910540-74:
(8*9)+(7*1)+(6*0)+(5*5)+(4*4)+(3*0)+(2*7)+(1*4)=138
138 % 10 = 8
So 910540-74-8 is a valid CAS Registry Number.

910540-74-8Downstream Products

910540-74-8Relevant academic research and scientific papers

Benzo[a]phenoselenazine-based NIR photosensitizer for tumor-targeting photodynamic therapy via lysosomal-disruption pathway

Gebremedhin, Kalayou H.,Li, Mingle,Gao, Fengli,Gurram, Bhaskar,Fan, Jiangli,Wang, Jingyun,Li, Yaming,Peng, Xiaojun

, (2019)

The ultimate goal of cancer therapy is to develop antitumor agents that will destroy selectively tumor cells while sparing the health cell of the patient. Herein, we reported a novel tumor-specific and lysosome dual-targeted NIR photosensitizer, Se-Biotin

Conditionally Activatable Photoredox Catalysis in Living Systems

Gebremedhin, Kalayou Hiluf,Kim, Jong Seung,Li, Mingle,Ma, Dandan,Peng, Xiaojun,Pu, Zhongji,Xiong, Tao,Xu, Yunjie

, p. 163 - 173 (2022/01/08)

The transformational effect of photoredox catalytic chemistries has inspired new opportunities, enabling us to interrogate nature in ways that are not possible otherwise and to unveil new biotechnologies in therapy and diagnosis. However, the deployment o

PHOTOSENSITIZER AND DERIVATIVES AND APPLICATION THEREOF

-

, (2021/02/05)

A photosensitizer and derivative, application thereof. The photosensitizer has the structure of general formula I, wherein X is S or Se, Y is organic or inorganic ion, R1 and R2 are independently selected from H, alkyl, alkoxy, alkyl

Improved synthetic method of Benzo[a]pheno-selenazinium phototherapeutic agents

Yue, Xiuxiu,Xu, Jing,Liu, Xiaozhong,Song, Xiangzhi,Foley, James W.

, (2021/01/25)

Benzo[a]phenoselenazinium dyes are excellent photodynamic therapeutic agents that have a red absorption (660 nm), high singlet oxygen quantum yield (>0.8), and good water-solubility and liposolubility. Bis-(3-diethylaminophenyl) diselenide, the most impor

Antimicrobial photoinactivation using chalcogen analogs of benzo(A)phenoxazinium dyes

-

Page/Page column 15, (2010/11/29)

Compositions and methods for the use of photoactivatable antimicrobial chalcogen analogs of benzophenoxazinium dyes in the treatment of infections are provided.

Synthesis and properties of benzo[a]phenoxazinium chalcogen analogues as novel broad-spectrum antimicrobial photosensitizers

Foley, James W.,Song, Xiangzhi,Demidova, Tatiana N.,Jilal, Fatima,Hamblin, Michael R.

, p. 5291 - 5299 (2007/10/03)

The goal of this investigation was to develop improved photosensitizers for use as antimicrobial drugs in photodynamic therapy of localized infections. Replacement of the oxygen atom in 5-(ethylamino)-9-diethylaminobenzo[a] phenoxazinium chloride (1) with

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