51671-03-5 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Dimethylnaphthalen-1-amine is used as a synthetic intermediate for the production of various pharmaceuticals. Its unique chemical properties allow it to be incorporated into the molecular structures of drugs, potentially enhancing their efficacy and therapeutic applications.
Used in Agrochemical Industry:
2,4-Dimethylnaphthalen-1-amine is used as a building block in the synthesis of agrochemicals, such as pesticides and herbicides. Its aromatic amine structure can be modified to create compounds with specific pesticidal or herbicidal properties, contributing to the development of more effective agricultural products.
Used in Organic Chemistry Research:
2,4-Dimethylnaphthalen-1-amine is used as a reagent in various organic chemistry reactions. Its versatility in forming different types of chemical bonds makes it a valuable tool for researchers in the field of organic synthesis, allowing them to explore new chemical pathways and create novel compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 51671-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,7 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51671-03:
(7*5)+(6*1)+(5*6)+(4*7)+(3*1)+(2*0)+(1*3)=105
105 % 10 = 5
So 51671-03-5 is a valid CAS Registry Number.
51671-03-5Relevant academic research and scientific papers
Kharraz,Uriac,Sinbandhit,Toupet
, p. 4423 - 4432 (1996)
Some 3H-1-benzazepines were prepared by dehydrogenation of secondary 2,3- and 2,5-dihydro-1H-1-benzazepines involving a hydride transfer to an iminium ion generated from a heterocylic enamine and BF3. With 2,5-dihydro-1H-1-benzazepines the initial formation of 5H-1-benzazepines was observed, whose treatment in the presence of BF3 led to 3H-1-benzazepines. The same rearrangement could be performed with t-BuOK. The hydride transfer was demonstrated using a deuterium labelled substrate. Tertiary dihydro-1-benzazepines was also oxidized but underwent rearrangement to naphthylamine derivatives.
