784107-79-5 Usage
Uses
Used in Pharmaceutical Industry:
3-Iodo-2,6-dimethylaniline is utilized as a key building block in organic synthesis for the development of pharmaceuticals. Its unique structure allows for the creation of various medicinal compounds, contributing to the advancement of drug discovery and therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Iodo-2,6-dimethylaniline serves as an essential intermediate in the synthesis of agrochemicals. Its incorporation into these products aids in the development of effective pesticides and other agricultural chemicals to protect crops and enhance yield.
Used in Dye and Pigment Manufacturing:
3-Iodo-2,6-dimethylaniline is employed as a crucial component in the production of dyes and pigments. Its chemical properties enable the creation of a wide range of colorants used in various industries, including textiles, plastics, and printing inks.
Used in Research and Development:
3-Iodo-2,6-dimethylaniline also plays a significant role in research and development settings. It is used in the exploration of new chemical reactions and the synthesis of novel organic compounds, furthering scientific understanding and innovation in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 784107-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,4,1,0 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 784107-79:
(8*7)+(7*8)+(6*4)+(5*1)+(4*0)+(3*7)+(2*7)+(1*9)=185
185 % 10 = 5
So 784107-79-5 is a valid CAS Registry Number.
784107-79-5Relevant academic research and scientific papers
BRIDGED, BICYCLIC HETEROCYCLIC OR SPIRO BICYCLIC HETEROCYCLIC DERIVATIVES OF PYRAZOLO[1,5-A]PYRIMIDINES, METHODS FOR PREPARATION AND USES THEREOF
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, (2009/10/21)
Compounds of formula A: Formula (1) pharmaceutically acceptable salts thereof are described, which selectively inhibit Raf kinase activity and are useful for treating disorders mediated by Raf kinases.
Preparation of axially chiral biphenyl diphosphine ligands and their application in asymmetric hydrogenation
Morimoto, Toshiaki,Yoshikawa, Kiyoshi,Murata, Masanao,Yamamoto, Naoko,Achiwa, Kazuo
, p. 1445 - 1450 (2007/10/03)
Axially chiral biphenyldiphosphine ligands bearing diphenylphosphino group(s) and/or dicyclohexylphosphino group(s) were prepared in enantiomerically pure form starting from 2,6-dimethylnitrobenzene via 8 steps: iodination, reduction, methoxylation throug
