761001-65-4 Usage
Uses
Used in Pharmaceutical Industry:
1-(3-Bromo-4-methylphenyl)piperidine serves as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with specific therapeutic targets, contributing to advancements in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(3-Bromo-4-methylphenyl)piperidine is utilized as a precursor in the production of pesticides and other agrochemicals. Its chemical properties make it suitable for the creation of effective and targeted pest control solutions.
Used in Drug Discovery and Development:
1-(3-Bromo-4-methylphenyl)piperidine is employed as a valuable component in drug discovery and development processes. Its structural attributes enable researchers to explore its potential in creating novel bioactive molecules with specific pharmacological effects.
Used in Synthesis of Bioactive Molecules:
1-(3-Bromo-4-methylphenyl)piperidine's piperidine ring structure makes 1-(3-Bromo-4-methylphenyl)piperidine a potentially useful compound in the synthesis of bioactive molecules. It can be incorporated into various chemical entities to enhance their biological activity and therapeutic potential.
The specific applications and uses of 1-(3-Bromo-4-methylphenyl)piperidine may vary depending on the industry and research area, highlighting its adaptability and importance in diverse fields of chemical and medicinal research.
Check Digit Verification of cas no
The CAS Registry Mumber 761001-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,1,0,0 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 761001-65:
(8*7)+(7*6)+(6*1)+(5*0)+(4*0)+(3*1)+(2*6)+(1*5)=124
124 % 10 = 4
So 761001-65-4 is a valid CAS Registry Number.
761001-65-4Relevant academic research and scientific papers
A Selective C?H Deprotonation Strategy to Access Functionalized Arynes by Using Hypervalent Iodine
Sundalam, Sunil K.,Nilova, Aleksandra,Seidl, Thomas L.,Stuart, David R.
, p. 8431 - 8434 (2016/07/19)
Described here is an efficient method to access highly functionalized arynes from unsymmetrical aryl(mesityl)iodonium tosylate salts. The iodonium salts are prepared in a single pot from either commercially available aryl iodides or arylboronic acids. The
NOVEL 3-(2-AMINO-4-PYRIMIDINYL)-4-HYDROXYPHENYL KETONE DERIVATIVES
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Page 45, (2010/02/08)
The present invention relates to novel compounds having 3-(2-amino-4-pyrimidinyl)-4-hydroxyphenyl ketone structure, as being illustrated in Formula 1, for inhibition of angiogenesis receptor tyrosine kinases, in particular, VEGF receptor 2 kinase ("KDR")
