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Triphenylstannanylium morpholine-4-carbodithioate, with the chemical formula (C6H5)3SnNMorphS2, is a coordination complex that consists of a triphenylstannanylium cation and a morpholine-4-carbodithioate anion. triphenylstannanylium morpholine-4-carbodithioate is recognized for its versatile applications in various fields, including medicine, materials science, and chemical research.

26879-88-9

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26879-88-9 Usage

Uses

Used in Chemical Synthesis:
Triphenylstannanylium morpholine-4-carbodithioate is used as a chemical intermediate and a catalyst in organic synthesis, facilitating various chemical reactions and improving the efficiency of synthesis processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, triphenylstannanylium morpholine-4-carbodithioate is studied for its potential use in anti-cancer therapies. It is being investigated for its ability to target and inhibit the growth of cancer cells, offering a promising avenue for the development of new cancer treatments.
Used as an Antimicrobial Agent:
Triphenylstannanylium morpholine-4-carbodithioate is also being explored for its antimicrobial properties, making it a potential candidate for use in applications that require the inhibition of microbial growth, such as in the development of new antibiotics or disinfectants.
Used in Enzyme Inhibition Research:
triphenylstannanylium morpholine-4-carbodithioate has been studied for its inhibitory effects on certain enzymes, which could have implications in the treatment of various diseases where enzyme regulation is critical.
Used in Materials Science:
Triphenylstannanylium morpholine-4-carbodithioate is being investigated for its potential use in the development of new materials, where its unique chemical properties could contribute to the creation of innovative materials with specific characteristics.
Used as a Reagent in Chemical Analysis:
In the field of chemical analysis, triphenylstannanylium morpholine-4-carbodithioate serves as a reagent, aiding in the identification, measurement, or testing of other substances in various analytical processes.
Overall, triphenylstannanylium morpholine-4-carbodithioate's diverse applications highlight its potential as a valuable compound in scientific and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 26879-88-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,8,7 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 26879-88:
(7*2)+(6*6)+(5*8)+(4*7)+(3*9)+(2*8)+(1*8)=169
169 % 10 = 9
So 26879-88-9 is a valid CAS Registry Number.

26879-88-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Stannane, [[morpholino(thiocarbonyl)]thio]triphenyl-

1.2 Other means of identification

Product number -
Other names triphenyl tin morpholyl dithiocarbamate

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:26879-88-9 SDS

26879-88-9Downstream Products

26879-88-9Relevant academic research and scientific papers

Synthesis, spectroscopic characterization, X-ray structure, and in vitro antitumor activities of new triorganotin(IV) complexes with sulfur donor ligand

Safari, Mojdeh,Yousefi, Mohammad,Jenkins, Hilary A.,Torbati, Maryam Bikhof,Amanzadeh, Amir

, p. 5730 - 5738 (2013)

The discovery of the anticancer properties of cisplatin promoted a great deal of interest in the area of metal-based antitumor agents. With this aim, a new series of triorganotin(IV) derivatives: Ph3SnL (1), BZ 3SnL (2), where L = morpholine-1-carbodithioate (MCDT) have been synthesized by the reaction of triorganotin(IV) chlorides with the ligand-salt in the appropriate molar ratio. All the complexes have been characterized by FT-IR, 1H, 13C, and 19Sn NMR spectroscopy. In addition, the molecular structure of complex 1 was determined by single crystal X-ray diffraction study. X-ray crystallographic analysis shows that in the compound [Ph3Sn(MCDT)], the Sn ion is in a four-coordinate environment with a dithiocarbamate ligand coordinated to the tin(IV) in a monodentate fashion through the sulfur atom. Furthermore, the cytotoxic activity of the free ligand (MCDT) as well as its triorganotin(IV) complexes were tested against tumor cell lines human cervix carcinoma HeLa, human myelogenous leukemia K562 and normal immunocompetent cells, peripheral blood mononuclear cells PBMC. The cytotoxic results indicate that coupling of MCDT with R 3Sn(IV) metal center results in a complex with important biological properties and remarkable cytotoxic activity, since we observe IC50 values better to that of the antitumor drug cisplatin.

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