191529-09-6 Usage
Description
2,4,6-Tribromobenzene-1,3,5-tricarbaldehyde is a chemical compound characterized by its molecular formula C9H3Br3O3. It features a symmetrical structure with three aldehyde groups positioned at the 1, 3, and 5 positions on a benzene ring, complemented by the presence of three bromine atoms at the 2, 4, and 6 positions. 2,4,6-tribromobenzene-1,3,5-tricarbaldehyde is known for its role in organic synthesis and as a precursor for the creation of more complex molecular structures.
Uses
Used in Organic Synthesis:
2,4,6-Tribromobenzene-1,3,5-tricarbaldehyde is utilized as a building block in organic synthesis for the construction of a variety of complex organic molecules. Its unique structure with aldehyde and bromine substituents allows for versatile chemical reactions and the formation of diverse molecular architectures.
Used in the Production of Coordination Complexes:
2,4,6-tribromobenzene-1,3,5-tricarbaldehyde serves as a reagent in the synthesis of coordination complexes, which are important in various fields such as catalysis, materials science, and medicinal chemistry. The presence of aldehyde groups and bromine atoms facilitates the formation of stable complexes with metal ions.
Used in Chemical Reactions as a Reagent:
2,4,6-Tribromobenzene-1,3,5-tricarbaldehyde is employed as a reagent in a range of chemical reactions, including condensation, oxidation, and reduction processes. Its functional groups enable it to participate in multiple types of chemical transformations, making it a valuable tool in the synthesis of new compounds.
Used in Materials Science:
2,4,6-tribromobenzene-1,3,5-tricarbaldehyde has potential applications in materials science, where its unique structure and properties can be harnessed to develop new materials with specific characteristics. These may include properties such as thermal stability, electrical conductivity, or optical properties, depending on the context of use.
Used in Environmental Analysis as a Reagent:
2,4,6-Tribromobenzene-1,3,5-tricarbaldehyde also finds use in environmental analysis, where it can act as a reagent to detect or quantify specific substances in environmental samples. Its chemical properties allow for selective reactions or interactions with target analytes, contributing to the development of sensitive and specific analytical methods.
Check Digit Verification of cas no
The CAS Registry Mumber 191529-09-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,5,2 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 191529-09:
(8*1)+(7*9)+(6*1)+(5*5)+(4*2)+(3*9)+(2*0)+(1*9)=146
146 % 10 = 6
So 191529-09-6 is a valid CAS Registry Number.
191529-09-6Relevant articles and documents
Interfacial synthesis of crystalline two-dimensional cyano-graphdiyne
Chen, Siqi,Li, Zhibo,Pan, Qingyan,Shao, Feng,Sun, Qingzhu,Wu, Chenyu,Zhang, Zhaohui,Zhao, Yingjie
supporting information, p. 3210 - 3213 (2020/03/23)
A well-defined crystalline cyano-functionalized graphdiyne (CN-GDY) is synthesized at a liquid/liquid interface through alkyne-alkyne coupling reactions. The configurations and nanostructures of CN-GDY were well characterized by TEM, SEM, AFM, XPS, and Raman spectroscopy. HR-TEM and selected area electron diffraction (SAED) in combination with structure simulation firmly revealed a 9-fold stacking mode for CN-GDY.
An efficient route to 1,3,5-triazido-2,4,6-tricyanobenzene
Becke, Martin,Voss, Karsten,Villinger, Alexander,Schulz, Axel
, p. 643 - 649,7 (2020/08/31)
An efficient synthetic route starting from 1,3,5-trimethylbenzene is described for binary 1,3,5- triazido-2,4,6-tricyanobenzene. Besides 1,3,5-triazido-2,4,6-tricyanobenzene, all intermediates have been isolated and fully characterized.
En route to archimedene: Total synthesis of C3h-symmetric [7]phenylene
Bruns, Dirk,Miura, Hirokazu,Vollhardt, K. Peter C.,Stanger, Amnon
, p. 549 - 552 (2007/10/03)
(Matrix presented) The total synthesis of C3h-symmetric [7]phenylene has been accomplished by triple cobalt-catalyzed cycloisomerization of an appropriate nonayne. Its spectral data are in accord with the expectations for a triply angularly fus
