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[(2,4,6-trioxo-1,3-diazinan-5-ylidene)amino]thiourea, with the molecular formula C3H5N5O3S, is a heterocyclic organic compound characterized by the presence of a diazinane ring and a thiourea functional group. [(2,4,6-trioxo-1,3-diazinan-5-ylidene)amino]thiourea is recognized for its diverse chemical reactivity and its ability to engage in a wide range of reactions, making it a valuable asset in the realm of organic chemistry.

6960-27-6

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6960-27-6 Usage

Uses

Used in Chemical Synthesis:
[(2,4,6-trioxo-1,3-diazinan-5-ylidene)amino]thiourea serves as a fundamental building block for the synthesis of other organic compounds. Its unique structure and reactivity allow it to be a key component in creating a variety of molecules with different properties and applications.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, [(2,4,6-trioxo-1,3-diazinan-5-ylidene)amino]thiourea has demonstrated potential as a therapeutic agent for the treatment of certain diseases. Its specific mode of action and interaction with biological targets are areas of ongoing research, with the aim of developing new drugs based on its chemical properties.
Used as a Reagent in Chemical Reactions:
Due to its diverse reactivity, [(2,4,6-trioxo-1,3-diazinan-5-ylidene)amino]thiourea is also utilized as a reagent in various chemical reactions. It can facilitate or catalyze specific transformations, making it a versatile tool for chemists working in different areas of research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 6960-27-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6960-27:
(6*6)+(5*9)+(4*6)+(3*0)+(2*2)+(1*7)=116
116 % 10 = 6
So 6960-27-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H5N5O3S/c6-4(14)10-9-1-2(11)7-5(13)8-3(1)12/h(H3,6,10,14)(H2,7,8,11,12,13)

6960-27-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2,4,6-trioxo-1,3-diazinan-5-ylidene)amino]thiourea

1.2 Other means of identification

Product number -
Other names 2-[2,4,6-trioxotetrahydropyrimidin-5(6H)-ylidene]hydrazinocarbothioamide

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:6960-27-6 SDS

6960-27-6Downstream Products

6960-27-6Relevant academic research and scientific papers

Identifying the therapeutic property of the synthesized schiff base ligand and its metal complex involving green technology

Priya, G. Padma,Girija,Sathish

, p. 3629 - 3643 (2020/12/03)

Schiff bases are aldehyde- or ketone-like compounds in which the carbonyl group is replaced by an imine or azomethine group. Schiff bases are adaptable ligands which are produced from the condensation of primary amines with carbonyl groups. Production of Schiff base transition metal complexes by using Schiff base as ligands seems to be enthralling in view of the opportunity of obtaining coordination compounds of unusual structure and steadiness. They are widely used for industrial purposes and also exhibit a broad range of biological activities. Characterization using UV, IR, NMR, Antibacterial, Docking studies of Schiff base and its metal complex is investigated. The biological activity of the transition metal complexes derived from the Schiff base ligands has been widely studied. This evaluation summarizes the importance, Scope and antimicrobial activities of Schiff base metal complexes.

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