34743-49-2 Usage
Description
4-methoxy-2,6-dimethyl-aniline is an aromatic amine and aniline derivative with the molecular formula C9H13NO. It is characterized by its methoxy and dimethyl substituents on the aromatic ring, which impart specific physical and chemical properties to the molecule. This chemical compound is commonly utilized as an intermediate in the synthesis of dyes, pharmaceuticals, and other organic compounds. However, it is important to handle 4-methoxy-2,6-dimethyl-aniline with caution, as exposure to this compound can cause irritation to the eyes, skin, and respiratory system, and may have potential harmful effects on human health and the environment.
Uses
Used in Dye Industry:
4-methoxy-2,6-dimethyl-aniline is used as a chemical intermediate for the synthesis of various dyes. Its unique structure and properties make it a valuable component in the production of a wide range of dyes with different color characteristics and properties.
Used in Pharmaceutical Industry:
4-methoxy-2,6-dimethyl-aniline is used as a building block in the synthesis of various pharmaceutical compounds. Its presence in the molecular structure can influence the pharmacological properties, such as solubility, stability, and bioavailability, of the final drug product.
Used in Organic Synthesis:
4-methoxy-2,6-dimethyl-aniline is used as a versatile intermediate in the synthesis of other organic compounds. Its reactivity and functional groups make it suitable for various organic reactions, such as substitution, addition, and condensation, leading to the formation of a diverse range of organic molecules with different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 34743-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,4 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34743-49:
(7*3)+(6*4)+(5*7)+(4*4)+(3*3)+(2*4)+(1*9)=122
122 % 10 = 2
So 34743-49-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO/c1-6-4-8(11-3)5-7(2)9(6)10/h4-5H,10H2,1-3H3
34743-49-2Relevant articles and documents
B(C6F5)3-Catalyzed C-H Alkylation of N-Alkylamines Using Silicon Enolates without External Oxidant
Chan, Jessica Z.,Chang, Yejin,Wasa, Masayuki
supporting information, p. 984 - 988 (2019/02/14)
An efficient method for the coupling of N-alkylamines with silicon enolates to generate β-amino carbonyl compounds is disclosed. These reactions proceed by activation of α-amino C-H bonds by B(C6F5)3, which likely generate
PYRAZOLOPYRIMIDINE DERIVATIVES, PREPARATION METHOD THEREOF, AND PHARMACEUTICAL COMPOSITION FOR USE IN PREVENTING OR TREATING CANCER, AUTOIMMUNE DISEASE AND BRAIN DISEASE CONTAINING THE SAME AS AN ACTIVE INGREDIENT
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Paragraph 628-632, (2018/12/02)
The present invention relates to a pyrazolopyrimidine derivative, a preparation method thereof and a pharmaceutical composition comprising the same as an active ingredient for the prevention or treatment of cancer, autoimmune disease and brain disease. The pyrazolopyrimidine derivative of the present invention exhibits excellent Bruton's tyrosine kinase inhibition activity, so that it can be effectively used as a pharmaceutical composition for the prevention or treatment of cancer, autoimmune disease and Parkinson's disease.
Efficient copper-catalyzed amination of DNA-conjugated aryl iodides under mild aqueous conditions
Ruff, Yves,Berst, Frédéric
supporting information, p. 1188 - 1193 (2018/08/01)
Herein, we describe the development of copper-catalyzed cross-coupling of DNA-conjugated aryl iodides with aliphatic amines. This protocol leverages a novel ligand, 2-((2,6-dimethoxyphenyl)amino)-2-oxoacetic acid, to effect the transformation in aqueous D