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8-benzyl-2-methyl-6-phenylimidazo[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.

70217-85-5

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70217-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70217-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,1 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70217-85:
(7*7)+(6*0)+(5*2)+(4*1)+(3*7)+(2*8)+(1*5)=105
105 % 10 = 5
So 70217-85-5 is a valid CAS Registry Number.

70217-85-5Relevant academic research and scientific papers

NOVEL COELENTERAZINE SUBSTRATES AND METHODS OF USE

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, (2012/05/20)

An isolated polynucleotide encoding a modified luciferase polypeptide and novel coelenterazine- based substrates. The OgLuc variant polypeptide has at least 60% amino acid sequence identity to SEQ ID NO: 1 and at least one amino acid substitution at a position corresponding to an amino acid in SEQ ID NO: 1. The OgLuc variant polypeptide has at least one of enhanced luminescence, enhanced signal stability, and enhanced protein stability relative to the corresponding polypeptide of the wild-type Oplophorus luciferase.

NOVEL COELENTERAZINE SUBSTRATES AND METHODS OF USE

-

, (2012/05/20)

An isolated polynucleotide encoding a modified luciferase polypeptide and novel coelenterazine-based substrates. The OgLuc variant polypeptide has at least 60% amino acid sequence identity to SEQ ID NO: 1 and at least one amino acid substitution at a position corresponding to an amino acid in SEQ ID NO: 1. The OgLuc variant polypeptide has at least one of enhanced luminescence, enhanced signal stability, and enhanced protein stability relative to the corresponding polypeptide of the wild-type Oplophorus luciferase.

Influence of electron-donating and electron-withdrawing substituents on the Chemiluminescence behavior of Coelenterazine analogs

Saito, Ryota,Hirano, Takashi,Maki, Shojiro,Niwa, Haruki,Ohashi, Mamoru

experimental part, p. 90 - 99 (2011/04/12)

Coelenterazine analogs 3a3e possessing various substituents at the para-position of the 6-phenyl group (R = CF3, F, H, OMe, and NMe 2) were synthesized, and the chemiluminescent properties of 3a3e in dimethyl sulfoxide (DMSO) were investigated quantitatively. Chemiluminescence maxima observed in the range of 454478nm showed a bathochromic shift as the electron-donating ability of R increased. Chemiluminescence quantum yields (φCL) were obtained in the range of 0.00060.0018. The analog 3a possessing the electron-withdrawing CF3 group showed a slight decrease in its φCL value. The fluorescence quantum yields (φF) of the light emitter, 2-acetamidopyrazine anions 4a --4e- , were observed in the range of 0.0050.21 and showed substituent dependency in that the increment in the electronwithdrawing ability of R decreases the φF value. The efficiency of generation of the singlet-excited 4a--4e- (φS) showed a small change in the range of 0.0080.015. From these quantitative analyses of the quantum efficiencies, we found that an electron-donating substituent R is not required for the efficient generation of a singlet-excited light emitter, but is required for the high φF of the emitter.

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