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Bis(2-quinolinyl)disulfide, also known as 1,1'-(Disulfanediyl)bis(2-quinoline), is an organic compound with the chemical formula C18H12N2S2. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol, acetone, and chloroform. bis(2-quinolinyl)disulfide is primarily used as a fluorescent probe in analytical chemistry, particularly for the detection of metal ions like copper and zinc. It exhibits strong fluorescence upon binding to these ions, making it a valuable tool in various research applications. Bis(2-quinolinyl)disulfide is also known for its potential use in the development of chemosensors and as a reagent in the synthesis of other organic compounds.

2889-13-6

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2889-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2889-13-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,8 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2889-13:
(6*2)+(5*8)+(4*8)+(3*9)+(2*1)+(1*3)=116
116 % 10 = 6
So 2889-13-6 is a valid CAS Registry Number.

2889-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2-quinolinyl)-disulfide

1.2 Other means of identification

Product number -
Other names 2,2'-bisquinolinyl disulfide

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

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

More Details:2889-13-6 SDS

2889-13-6Relevant academic research and scientific papers

Reaction of 2-quinolyl thiocyanate with C-nucleophiles

Iijima,Hiyoshi,Miyashita

, p. 1090 - 1093 (2007/10/02)

2-Quinolyl thiocyanate (2) was found to react with C-nucleophiles, i.e., phenylacetonitrile, p-chlorophenylacetonitrile, p-cyanophenylacetonitrile, p-methoxyphenylacetonitrile, ethyl cyanoacetate, and malononitrile, in two ways, depending on the nature of

REAKTIONEN VON THIOXOHETEROCYCLEN MIT N-CHLORAMIDEN III. 2- ODER 4-THIOPYRIDONE OHNE SUBSTITUENTEN AM STICKSTOFF UND NATRIUM-N-CHLORBENZOLSULFONAMIDE

Boberg, Friedrich,Bruchmann, Bernd,Garming, Alfons,Nink, Gunter

, p. 313 - 326 (2007/10/02)

2- and 4-pyridinethiones (A) react with sodium N-chlorobenzenesulfonamides (1) in alcoholic solvents to N-(pyridylthio)benzenesulfonamides (C), sodium N,N'-bis(phenylsulfonyl)-S-pyridylsulfodiimidates (D) and S-alkoxy-N-phenylsulfonyl-S-pyridylsulfimides (E).Constitution proofs for the new compounds D, E are reactions and 1H-, 13C-, 15N-nmr data.

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