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65726-66-1

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65726-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65726-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,2 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65726-66:
(7*6)+(6*5)+(5*7)+(4*2)+(3*6)+(2*6)+(1*6)=151
151 % 10 = 1
So 65726-66-1 is a valid CAS Registry Number.

65726-66-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1,4-dioxonaphthalen-2-yl)sulfanylpropanoic acid

1.2 Other means of identification

Product number -
Other names 3-(1,4-dioxo-1,4-dihydro-[2]naphthylsulfanyl)-propionic acid

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:65726-66-1 SDS

65726-66-1Downstream Products

65726-66-1Relevant articles and documents

Benzoquinone and naphthoquinone based redox-active labels for electrochemical detection of modified oligonucleotides on Au electrodes

Shundrin, Leonid A.,Irtegova, Irina G.,Vasilieva, Nadezhda V.,Khalfina, Irina A.

supporting information, p. 392 - 395 (2016/01/12)

The reaction of 1,4-benzoquinone and 1,4-naphthoquinone with β-thiopropionic acid yielded 3-[(3,6-dioxocyclohexa-1,4-diene-1-yl)thio]propionic and 3-[(1,4-dioxo-1,4-dihydronaphthalene-2-yl)thio]propionic acids, respectively. These compounds were used to modify oligonucleotides to allow their electrochemical detection on the surface of Au electrodes using cyclic voltammetry. Electrochemical reduction of the corresponding amides, modeling the bonding of the redox-active labels with molecules that are not electrochemically active, was also studied.

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