133735-81-6 Usage
Chemical structure
The compound has a triazole ring and a benzyl group attached to it, with two diethoxymethyl groups in its molecular structure.
Functional groups
Contains a triazole ring, benzyl group, and diethoxymethyl groups.
Molecular weight
Approximately 287.36 g/mol (calculated from the molecular formula).
Appearance
The compound is likely a solid, although the specific appearance is not provided in the material.
Solubility
The solubility of the compound is not mentioned in the material, but it may be soluble in organic solvents due to its nonpolar nature.
Stability
The stability of the compound is not explicitly mentioned, but it is likely stable under normal conditions due to its covalent bonding.
Reactivity
The compound is used as an intermediate in organic synthesis, indicating that it is reactive in various chemical reactions.
Applications
Potential applications in medicinal chemistry and material science due to its unique structure and properties.
Safety precautions
It is important to handle and store this chemical with caution as it may pose health and safety risks if not properly managed. Specific hazards are not provided in the material, but general chemical safety practices should be followed.
Check Digit Verification of cas no
The CAS Registry Mumber 133735-81-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,7,3 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 133735-81:
(8*1)+(7*3)+(6*3)+(5*7)+(4*3)+(3*5)+(2*8)+(1*1)=126
126 % 10 = 6
So 133735-81-6 is a valid CAS Registry Number.
133735-81-6Relevant articles and documents
Reusable polymer-supported catalyst for the [3+2] Huisgen cycloaddition in automation protocols
Girard, Christian,Oenen, Esra,Aufort, Marie,Beauviere, Sophie,Samson, Edmond,Herscovici, Jean
, p. 1689 - 1692 (2006)
A polymer-supported catalyst for Huisgen's [3+2] cycloaddition reaction between azides and alkynes was prepared from copper(I) iodide and Amberlyst A-21. This catalyst was then used in an automated synthesis of 1,4-disubstituted 1,2,3-triazoles giving acc
Bio-waste corn-cob cellulose supported poly(hydroxamic acid) copper complex for Huisgen reaction: Waste to wealth approach
Mandal, Bablu Hira,Rahman, Md. Lutfor,Yusoff, Mashitah Mohd,Chong, Kwok Feng,Sarkar, Shaheen M.
, p. 175 - 181 (2016/09/23)
Corn-cob cellulose supported poly(hydroxamic acid) Cu(II) complex was prepared by the surface modification of waste corn-cob cellulose through graft copolymerization and subsequent hydroximation. The complex was characterized by IR, UV, FESEM, TEM, XPS, E
One-pot synthesis of TBTA-functionalized coordinating polymers
Movahedi, Alireza,Moth-Poulsen, Kasper,Ekl?f, Johnas,Nydén, Magnus,Kann, Nina
, p. 1 - 8 (2014/06/24)
A one-pot method for the functionalization of polyvinylbenzyl chloride with a tris-(benzyltriazolylmethyl)amine (TBTA) ligand via the copper-catalyzed azide-alkyne cycloaddition reaction (CuAAC) is reported, where the ligand is constructed simultaneously
