3096-71-7 Usage
Description
4-Amino-2,5-dimethylphenol is an organic compound characterized by its solid state and a unique molecular structure featuring an amino group and two methyl groups attached to a phenol ring. 4-Amino-2,5-dimethylphenol is known for its potential applications in various fields due to its chemical properties.
Uses
Used in Chemical Synthesis Studies:
4-Amino-2,5-dimethylphenol is used as a chemical intermediate for the synthesis of various compounds. Its unique structure allows it to be a versatile building block in the creation of different organic molecules, contributing to the development of new materials and pharmaceuticals.
Used in Pharmaceutical Industry:
4-Amino-2,5-dimethylphenol is used as a key component in the development of pharmaceuticals, particularly those targeting specific medical conditions. Its chemical properties make it a valuable asset in the design and synthesis of novel drug molecules.
Used in Material Science:
In the field of material science, 4-Amino-2,5-dimethylphenol is used as a precursor for the development of advanced materials with specific properties. Its solid-state structure and reactivity contribute to the creation of materials with tailored characteristics for various applications.
Used in Analytical Chemistry:
4-Amino-2,5-dimethylphenol is utilized as a reference compound or standard in analytical chemistry for the calibration of instruments and the development of new analytical methods. Its distinct chemical properties make it suitable for these purposes, ensuring accurate and reliable results in chemical analysis.
Check Digit Verification of cas no
The CAS Registry Mumber 3096-71-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,9 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3096-71:
(6*3)+(5*0)+(4*9)+(3*6)+(2*7)+(1*1)=87
87 % 10 = 7
So 3096-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO/c1-5-4-8(10)6(2)3-7(5)9/h3-4,10H,9H2,1-2H3
3096-71-7Relevant articles and documents
TRANSITION METAL FREE METHODS OF SYNTHESIS OF BIARYL COMPOUNDS
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Page/Page column 74; 75, (2017/06/21)
The present disclosure provides methods of preparing biaryl compounds which do not require transition metal catalysts. In yet another aspect, the present disclosure provides pharmaceutical compositions comprising compounds as described herein and pharmaceutically acceptable carriers.
The Diels-Alder reactions of para-benzoquinone nitrogen-derivatives: An experimental and theoretical study
Uliana, Marciana P.,Servilha, Bruno M.,Alexopoulos, Olga,De Oliveira, Kleber T.,Tormena, Cláudio F.,Ferreira, Marco A.B.,Brocksom, Timothy J.
, p. 6963 - 6973 (2015/11/09)
An experimental and theoretical study of the comparative reactivity and selectivity of the Diels-Alder reactions of para-benzoquinones and three nitrogen derivatives have been performed. The mono-oximes derivatives do not react under the tested reaction conditions, whereas the tosylated mono-oximes react slowly. However, the mono N-tosyl imines show excellent reactivity, and superior to the parent parabenzoquinones. DFT calculations support these experimental results.
Hair colouring and conditioning compositions
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, (2008/06/13)
A hair colouring and conditioning composition comprising: (a) a hair colouring agent; and (b) a hair conditioning agent; wherein the composition provides an Average Combing Index Value of greater than 1.2 as measured by the Combing Technical Test Method. The products can provide excellent hair colouring together with excellent conditioning, reduced hair damage, brittleness and dryness, and is convenient and easy to use.