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Piperidine, 1,1'-(1,2-dithioxo-1,2-ethanediyl)bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24528-76-5

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24528-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24528-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,2 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24528-76:
(7*2)+(6*4)+(5*5)+(4*2)+(3*8)+(2*7)+(1*6)=115
115 % 10 = 5
So 24528-76-5 is a valid CAS Registry Number.

24528-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-di(piperidin-1-yl)ethane-1,2-dithione

1.2 Other means of identification

Product number -
Other names 1,1'-dithiooxalyl-bis-piperidine

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:24528-76-5 SDS

24528-76-5Relevant academic research and scientific papers

Cp and indenyl ruthenium complexes containing dithione derivatives: Synthesis, antibacterial and antifungal study

Dkhar, Lincoln,Joshi, Santa Ram,Ka-Ot, Agustine Lamin,Kaminsky, Werner,Kollipara, Mohan Rao,Sawkmie, Merrily

, (2020)

A series of cationic complexes [(Cp/Ind)Ru(к2(SS)-L)(PPh3)]PF6 (1–6) are obtained by the reaction of [CpRu(PPh3)2Cl] or [(Ind)Ru(PPh3)2Cl] (Cp = η5-C5H5, Ind = η5-C9H7) with respective dithione derivatives 1,2-di(piperidin-1-yl)ethane-1,2-dithione (L1), 1,2-dimorpholinoethane-1,2-dithione (L2) and 1,2-dithiomorpholinoethane-1,2-dithione (L3). All the compounds are characterized using spectroscopic techniques. The molecular structures of complexes 1, 2 and 4 are established by single-crystal X-ray diffraction studies. Antimicrobial studies were tested against three strains of bacterial microorganisms Staphylococcus aureus (gram + ve), Bacillus subtilis (gram + ve), Klebsiella pneumoniae (gram -ve) and one strain of fungal microorganism Candida albicans.

Synthesis of N,N'-Disubstituted Dithiooxamide Derivatives by the Modified Willgerodt–Kindler Reaction

Boyarskii, V. P.,Eliseenkov, E. V.,Petrov, A. A.,Ponomareva, T. N.

, p. 781 - 787 (2020/07/03)

Abstract: The conditions of the reaction of trichloroethylene with sulfur and amines were optimized (the modified Willgerodt–Kindler reaction). The reaction of tetrachloroethylene with sulfur and some basic primary and secondary amines of the aliphatic series in DMF under mild conditions leads to N,N'-disubstituted dithiooxamides in 30–70% yields and with a 100% conversion of tetrachloroethylene.

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