3535-88-4 Usage
Description
2-Amine-4-tert-butylanisole, also known as 5-tert-Butyl-o-anisidine, is an organic compound with the chemical formula C11H17NO. It is characterized by the presence of an amine group (-NH2) attached to a tert-butyl group (-C(CH3)3) and an anisole moiety (-OCH3) attached to a phenyl ring. This unique structure endows it with specific chemical properties and potential applications in various fields.
Uses
Used in Chemical Synthesis Industry:
2-Amine-4-tert-butylanisole is used as a key intermediate in the synthesis of complex organic compounds and ligands. Its unique structure allows it to act as a building block for the development of new molecules with specific properties and functions.
Used in Coordination Chemistry:
2-Amine-4-tert-butylanisole is used as a potential tetradentate ligand for the preparation of anisole-containing polypyridylamine. This ligand can form stable complexes with metal ions, which can be employed in various applications, such as catalysis, sensors, and materials science.
Used in Pharmaceutical Industry:
Due to its ability to form stable complexes with metal ions, 2-Amine-4-tert-butylanisole can be used in the development of metal-based drugs. These drugs can target specific biological processes and have potential applications in the treatment of various diseases.
Used in Analytical Chemistry:
2-Amine-4-tert-butylanisole can be used as a chelating agent in analytical chemistry for the selective detection and quantification of metal ions. Its ability to form stable complexes with metal ions can improve the sensitivity and selectivity of analytical methods.
Used in Material Science:
The unique structure of 2-Amine-4-tert-butylanisole allows it to be used in the development of new materials with specific properties. For example, it can be incorporated into polymers to improve their stability, solubility, or mechanical properties, or it can be used to create metal-organic frameworks with potential applications in gas storage, catalysis, or drug delivery.
Check Digit Verification of cas no
The CAS Registry Mumber 3535-88-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,3 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3535-88:
(6*3)+(5*5)+(4*3)+(3*5)+(2*8)+(1*8)=94
94 % 10 = 4
So 3535-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO/c1-11(2,3)8-5-6-10(13-4)9(12)7-8/h5-7H,12H2,1-4H3
3535-88-4Relevant articles and documents
Photocatalytic C-H Amination of Aromatics Overcoming Redox Potential Limitations
Ikarashi, Gun,Kano, Naokazu,Morofuji, Tatsuya
supporting information, p. 2822 - 2827 (2020/04/16)
We report the photocatalytic C-H amination of aromatics overcoming redox potential limitations. Radical cations of aromatic compounds are generated photocatalytically using Ru(phen)3(PF6)2, which has a reduction potential at a high oxidation state (Ered(RuIII/RuII) = +1.37 V vs SCE) lower than the oxidation potentials of aromatic substrates (Eox = +1.65 to +2.27 V vs SCE). The radical cations are trapped with pyridine to give N-arylpyridinium ions, which were converted to aromatic amines.
