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Triphenylstannanylium piperidine-1-carbodithioate is a chemical compound that comprises a triphenylstannanylium cation and a piperidine-1-carbodithioate anion. The triphenylstannanylium cation features three phenyl groups bonded to a tin atom, and the piperidine-1-carbodithioate anion includes a piperidine ring with a carbodithioate functional group. triphenylstannanylium piperidine-1-carbodithioate is recognized for its utility in organic synthesis, especially in the creation of carbon-sulfur bonds, and it also exhibits potential antimicrobial and anticancer properties. However, due to its toxicity and possible environmental effects, careful handling and use are essential.

59086-70-3

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59086-70-3 Usage

Uses

Used in Organic Synthesis:
Triphenylstannanylium piperidine-1-carbodithioate is used as a reagent for the formation of carbon-sulfur bonds, which is crucial in the synthesis of various organic compounds.
Used in Antimicrobial Applications:
Triphenylstannanylium piperidine-1-carbodithioate is used as an antimicrobial agent, leveraging its potential to inhibit the growth of microorganisms, which can be beneficial in various industries such as pharmaceuticals and healthcare.
Used in Anticancer Applications:
Triphenylstannanylium piperidine-1-carbodithioate is used as a potential anticancer agent, with research indicating that it may have an impact on cancer cell growth and proliferation, making it a subject of interest for cancer research and therapeutic development.
Used in Environmental Remediation:
Although its toxicity and environmental impact are a concern, triphenylstannanylium piperidine-1-carbodithioate's properties may also be harnessed for environmental remediation purposes, such as in the detoxification of certain pollutants, under controlled and safe conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 59086-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,8 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59086-70:
(7*5)+(6*9)+(5*0)+(4*8)+(3*6)+(2*7)+(1*0)=153
153 % 10 = 3
So 59086-70-3 is a valid CAS Registry Number.

59086-70-3SDS

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 Stannane, triphenyl[[piperidino(thiocarbonyl)]thio]-

1.2 Other means of identification

Product number -
Other names triphenyl tin piperidyl 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:59086-70-3 SDS

59086-70-3Downstream Products

59086-70-3Relevant academic research and scientific papers

Synthesis of N,N-dialkyl dithiocarbamate triphenyltin(IV) and crystal structures of Ph3SnS2CN(C2H5)2 and Ph3SnS2CN(C5H10)

Zhu, Dezhong,Zhang, Rufen,Ma, Chunlin,Yin, Handong

, p. 1634 - 1638 (2007/10/03)

Eleven triphenyltin(IV) complexes with N,N-dialkyl dithiocarbamate ligands have been synthesized by the reaction of triphenyltin chloride with N,N-dialkyl dithiocarbamates and characterized by elemental analysis, UV, IR and 1H NMR. The crystal structures of Ph3SnS2CN(C2Hs)2 and Ph3SnS2CN(C5H10) have been determined by X-ray single crystal diffraction, their structures show a distorted trigonal bipyramidal configuration with five-coordination for the central tin atoms.

Synthesis and spectroscopic characterization of heterocyclic dithiocarbamate complexes of triorganotin (IV)

Sharma, Jyoti,Singh, Yashpal,Rai, Audhesh Kumar

, p. 19 - 26 (2007/10/03)

Heterocyclic dithiocarbamate complexes of triorganotin (IV) having general formula, CH2CH2XCH2CH2NCS2SnR 3 (where X = >CH2, >CH-CH3, >N-CH3, >O; R = -CHsub

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