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2-benzyl-6-phenyl-8-(phenylthio)imidazo[1,2-a]pyrazin-3(7H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1262117-93-0

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1262117-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1262117-93-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,1,1 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1262117-93:
(9*1)+(8*2)+(7*6)+(6*2)+(5*1)+(4*1)+(3*7)+(2*9)+(1*3)=130
130 % 10 = 0
So 1262117-93-0 is a valid CAS Registry Number.

1262117-93-0Downstream Products

1262117-93-0Relevant articles and documents

A novel coelenterate luciferin-based luminescent probe for selective and sensitive detection of thiophenols

Yuan, Mingliang,Ma, Xiaojie,Jiang, Tianyu,Zhang, Chaochao,Chen, Hui,Gao, Yuqi,Yang, Xingye,Du, Lupei,Li, Minyong

, p. 10267 - 10274 (2016)

The first dual bioluminescent and chemiluminescent sensor for detecting highly toxic thiophenols has been developed. Such a probe was designed by using a coelenterazine analogue as the luminophore and dinitrophenyl ether as the recognition moiety. It shou

Luminescence of coelenterazine derivatives with C-8 extended electronic conjugation

Yuan, Ming-Liang,Jiang, Tian-Yu,Du, Lu-Pei,Li, Min-Yong

, p. 550 - 554 (2016/04/26)

Replacement of the methylene group at the C-8 position with an extended electronic conjugation is a new promising method to develop red-shifted coelenterazine derivatives. In this paper, we have described an oxygen-containing coelenterazine derivative with a significant red-shifted (63 nm) bioluminescence signal maximum relative to coelenterazine 400a (DeepBlueC, 1). In cell imaging, the sulfur-containing coelenterazine derivative displayed a significantly (1.77 ± 0.09; P ≤ 0.01) higher luminescence signal compared to coelenterazine 400a and the oxygen-containing coelenterazine derivative exhibited a slightly (0.74 ± 0.08; P ≤ 0.05) lower luminescence signal. It is beneficial to understand further the underlying mechanisms of bioluminescence.

New red-shifted coelenterazine analogues with an extended electronic conjugation

Giuliani, Germano,Molinari, Paola,Ferretti, Giulia,Cappelli, Andrea,Anzini, Maurizio,Vomero, Salvatore,Costa, Tommaso

experimental part, p. 5114 - 5118 (2012/10/07)

A new promising approach to the development of red-shifted coelenterazine analogues was described. In order to alter the photochemical properties of native coelenterazine, we have designed and synthesized analogues bearing a new electron-rich structure. T

IMIDAZO[1,2-α]PYRAZIN-3(7H)-ONE DERIVATIVES BEARING A NEW ELECTRON-RICH STRUCTURE

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Page/Page column 39-40, (2011/02/24)

The present invention relates to compound of formula I : and their use as chemiluminescent and/or bioluminescent reagents.

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