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51583-69-8

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51583-69-8 Usage

General Description

2-Methyl-1-(3-sulphonatopropyl)quinolinium is a chemical compound with the formula C13H16NO3S. It is a quinolinium derivative with a methyl group at the 2-position and a sulphonatopropyl group at the 1-position. This chemical is often used as a fluorescent probe for detecting nucleic acids and proteins due to its unique structural and spectral properties. It can be utilized in biological and medical research to track specific molecules and study cellular processes. Additionally, it has potential applications in pharmaceuticals and diagnostics due to its ability to bind and interact with biomolecules. Overall, 2-Methyl-1-(3-sulphonatopropyl)quinolinium is a versatile compound with significant potential in various scientific and applied fields.

Check Digit Verification of cas no

The CAS Registry Mumber 51583-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,8 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51583-69:
(7*5)+(6*1)+(5*5)+(4*8)+(3*3)+(2*6)+(1*9)=128
128 % 10 = 8
So 51583-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO3S/c1-11-7-8-12-5-2-3-6-13(12)14(11)9-4-10-18(15,16)17/h2-3,5-8H,4,9-10H2,1H3

51583-69-8SDS

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 2-Methyl-1-(3-sulphonatopropyl)quinolinium

1.2 Other means of identification

Product number -
Other names 3-(2-methylquinolin-1-ium-1-yl)propane-1-sulfonate

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:51583-69-8 SDS

51583-69-8Downstream Products

51583-69-8Relevant articles and documents

Crown-ether styryl dyes 15. Synthesis and two pathways of regio- and stereospecific cation-dependent -autophotocycloaddition of chromogenic 15-crown-5-ether betaines of quinoline series

Gromov, S. P.,Fedorova, O. A.,Ushakov, E. N.,Buevich, A. V.,Alfimov, M. V.

, p. 2131 - 2136 (1995)

Styryl dyes (4a,b) containing a 15-crown-5 fragment and isomeric 2- and 4-quinolinium residues with an N-sulfopropyl substituent undergo -autophotocycloaddition to give cyclobutane derivatives (9a,b) in acetonitrile only in the presence of Mg(ClO4)2 or Ca(ClO4)2.The stereospecificity of both pathways of photocycloaddition and its efficiency are explained by the preorganization of the supramolecular dimers derived from the trans-isomers of the dyes when they are bound into complexes with Mg and Ca cations. - Keywords: crown ether styryl dyes; complex formation; -photocycloaddition; cyclobutane derivatives; 1H NMR spectra.

Microwave assisted sulfopropylation of N-heterocycles using 1,3-propane sultone

Adamczyk, Maciej,Rege, Sushil

, p. 9587 - 9588 (2007/10/03)

Dramatic rate acceleration was observed for N-sulfopropylation of heterocyclic compounds (1a-h) using 1,3-propane sultone(2) under microwave irradiation affording the N-sulfopropylated compounds (3a-h) in 68-95% yield.

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