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Imidazo[1,2-a]pyrazin-3-ol, 6-[4-(acetyloxy)phenyl]-2-[[4-(acetyloxy)phenyl]methyl]-8-(phenylmethyl)-, acetate (ester) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65417-16-5

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65417-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65417-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,1 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65417-16:
(7*6)+(6*5)+(5*4)+(4*1)+(3*7)+(2*1)+(1*6)=125
125 % 10 = 5
So 65417-16-5 is a valid CAS Registry Number.

65417-16-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name imidazo[1,2-a]pyrazin-3-ol,6-[4-(acetyloxy)phenyl]-2-[[4-(acetyloxy)phenyl]methyl]-8-(phenylmethyl)-3-acetate

1.2 Other means of identification

Product number -
Other names 3-acetoxy-2-(4-acetoxy-benzyl)-6-(4-acetoxy-phenyl)-8-benzyl-imidazo[1,2-a]pyrazine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65417-16-5 SDS

65417-16-5Relevant academic research and scientific papers

IMIDAZOPYRAZINE DERIVATIVES, PROCESS FOR PREPARATION THEREOF, AND THEIR USES AS LUCIFERINS

-

Page/Page column 120, (2018/11/22)

The present invention is in the field of bioluminescence in biology and/or medicine. In particular, the invention provides imidazopyrazine derivatives, processes for preparation thereof, and their uses as luciferins.

Development of luminescent coelenterazine derivatives activatable by β-galactosidase for monitoring dual gene expression

Lindberg, Eric,Mizukami, Shin,Ibata, Keiji,Miyawaki, Atsushi,Kikuchi, Kazuya

supporting information, p. 14970 - 14976 (2013/11/06)

Two bioluminogenic caged coelenterazine derivatives (bGalCoel and bGalNoCoel) were designed and synthesized to detect β-galactosidase activity and expression by means of bioluminescence imaging. Our approach addresses the instability of coelenterazine by introducing β-galactose caging groups to block the auto-oxidation of coelenterazine. Both probes contain β-galactosidase cleavable caging groups at the carbonyl group of the imidazo-pyrazinone moiety. One of the probes in particular, bGalNoCoel, displayed a fast cleavage profile, high stability, and high specificity for β-galactosidase over other glycoside hydrolases. bGalN-oCoel could detect β-galactosidase activity in living HEK-293T cell cultures that expressed a mutant Gaussia luciferase. It was determined that coelenterazine readily diffuses in and out of cells after uncaging by β-galactosidase. We showed that this new caged coelenterazine derivative, bGalNoCoel, could function as a dual-enzyme substrate and detect enzyme activity across two separate cell populations. Copyright

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