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Dichloridophosphoric acid 4-methyl-2-oxo-2H-1-benzopyran-7-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63468-52-0

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63468-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63468-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,6 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63468-52:
(7*6)+(6*3)+(5*4)+(4*6)+(3*8)+(2*5)+(1*2)=140
140 % 10 = 0
So 63468-52-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H7Cl2O4P/c1-6-4-10(13)15-9-5-7(2-3-8(6)9)16-17(11,12)14/h2-5H,1H3

63468-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-dichlorophosphoryloxy-4-methylchromen-2-one

1.2 Other means of identification

Product number -
Other names Phosphorodichloridic acid,4-methyl-2-oxo-2H-1-benzopyran-7-yl ester

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:63468-52-0 SDS

63468-52-0Downstream Products

63468-52-0Relevant academic research and scientific papers

Catalytic signal amplification for the discrimination of ATP and ADP using functionalised gold nanoparticles

Pezzato, Cristian,Chen, Jack L.-Y.,Galzerano, Patrizia,Salvi, Michela,Prins, Leonard J.

, p. 6811 - 6820 (2016)

Diagnostic assays that incorporate a signal amplification mechanism permit the detection of analytes with enhanced selectivity. Herein, we report a gold nanoparticle-based chemical system able to differentiate ATP from ADP by means of catalytic signal amplification. The discrimination between ATP and ADP is of relevance for the development of universal assays for the detection of enzymes which consume ATP. For example, protein kinases are a class of enzymes critical for the regulation of cellular functions, and act to modulate the activity of other proteins by transphosphorylation, transferring a phosphate group from ATP to give ADP as a byproduct. The system described here exploits the ability of cooperative catalytic head groups on gold nanoparticles to very efficiently catalyze chromogenic reactions such as the transphosphorylation of 2-hydroxypropyl-4-nitrophenyl phosphate (HPNPP). A series of chromogenic substrates have been synthesized and evaluated by means of Michaelis-Menten kinetics (compounds 2, 4-6). 2-Hydroxypropyl-(3-trifluoromethyl-4-nitro)phenyl phosphate (5) was found to display higher reactivity (kcat) and higher binding affinity (KM) when compared to HPNPP. This higher binding affinity allows phosphate 5 to compete with ATP and ADP to different extents for binding on the monolayer surface, thus enabling a catalytically amplified signal only when ATP is absent. Overall, this represents a viable new approach for monitoring the conversion of ATP into ADP with high sensitivity.

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