69125-10-6 Usage
Description
6-chloro-1,3,5-triazine-2,4(1H,3H)-dione, also known as a dihydroxy-1,3,5-triazine, is a chemical compound characterized by a 1,3,5-triazine-2,4-diol structure with a chloro group substitution at the 6th position. This molecule exhibits unique chemical properties due to its triazine core and functional groups, making it a versatile compound for various applications.
Uses
Used in Chemical Synthesis:
6-chloro-1,3,5-triazine-2,4(1H,3H)-dione is used as a synthetic building block for the development of new chemical compounds, particularly in the pharmaceutical and agrochemical industries. Its unique structure allows for the creation of a wide range of derivatives with diverse biological activities and properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-chloro-1,3,5-triazine-2,4(1H,3H)-dione is used as an intermediate in the synthesis of various therapeutic agents. Its chemical versatility enables the development of drugs with specific target profiles, potentially leading to novel treatments for various diseases and conditions.
Used in Agrochemical Industry:
6-chloro-1,3,5-triazine-2,4(1H,3H)-dione is also utilized in the agrochemical industry as a precursor for the development of new pesticides and herbicides. Its structural properties allow for the creation of compounds with enhanced efficacy and selectivity, contributing to more effective and environmentally friendly agricultural practices.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 6-chloro-1,3,5-triazine-2,4(1H,3H)-dione is used as a key component in the synthesis of various colorants. Its unique chemical structure contributes to the development of dyes and pigments with improved colorfastness, stability, and performance characteristics.
Used in Material Science:
6-chloro-1,3,5-triazine-2,4(1H,3H)-dione is employed in material science as a component in the development of advanced materials with specific properties, such as high thermal stability, flame retardancy, or UV resistance. Its incorporation into polymeric materials can lead to the creation of novel materials with enhanced performance characteristics for various applications.
Used in Environmental Applications:
6-chloro-1,3,5-triazine-2,4(1H,3H)-dione is used in environmental applications, such as water treatment and soil remediation, due to its ability to form complexes with heavy metal ions. This property allows for the removal of toxic metals from contaminated environments, contributing to cleaner and safer ecosystems.
Check Digit Verification of cas no
The CAS Registry Mumber 69125-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,2 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69125-10:
(7*6)+(6*9)+(5*1)+(4*2)+(3*5)+(2*1)+(1*0)=126
126 % 10 = 6
So 69125-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C3H2ClN3O2/c4-1-5-2(8)7-3(9)6-1/h(H2,5,6,7,8,9)
69125-10-6Relevant articles and documents
Synthesis and biological evaluation of lisofylline (LSF) analogs as a potential treatment for Type 1 diabetes
Cui, Peng,Macdonald, Timothy L.,Chen, Meng,Nadler, Jerry L.
, p. 3401 - 3405 (2007/10/03)
Lisofylline (LSF, 1-(5-R-hydroxyhexyl)-3,7-dimethylxanthine) is an anti-inflammatory agent that protects β-cells from Th1 cytokine-induced dysfunction and reduces the onset of Type 1 diabetes in non-obese diabetic (NOD) mice. Due to its low potency, poor oral bioavailability, and short half-life, the widespread clinical utility of LSF may be limited. Our goal has been to develop new agents based on the LSF structural motif that resolve the potency and pharmacokinetic liabilities of LSF. In this study, we have generated a focused library of LSF analogs that maintain the side chain (5-R-hydroxyhexyl) constant, while substituting a variety of nitrogen-containing heterocyclic substructures for the xanthine moiety of LSF. This library includes the xanthine-like (5-aza-7-deazaxanthine), as well as non-xanthine-like skeletons. The LSF analogs were evaluated in a pancreatic β-cell line for the effects on apoptosis protection and insulin release. The metabolic stability of selected compounds was also tested.
