99983-26-3 Usage
Uses
Used in Organic Chemistry:
4-(2-bromophenyl)piperidine-2,6-dione is used as a building block for the synthesis of various organic compounds. Its properties and reactivity contribute to its versatility in the production of a wide range of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(2-bromophenyl)piperidine-2,6-dione is used as an intermediate for the development of new drugs. Its unique structure and reactivity make it a valuable compound for medicinal chemistry and drug discovery.
Used in Agrochemical Industry:
4-(2-bromophenyl)piperidine-2,6-dione is also utilized in the agrochemical industry for the synthesis of various agrochemicals, contributing to the development of new products for agricultural applications.
Overall, 4-(2-bromophenyl)piperidine-2,6-dione is a valuable compound with diverse industrial and scientific uses, particularly in the fields of organic chemistry, pharmaceuticals, and agrochemicals. Its potential applications in medicinal chemistry and drug discovery further highlight its importance in the development of new and innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 99983-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,9,8 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 99983-26:
(7*9)+(6*9)+(5*9)+(4*8)+(3*3)+(2*2)+(1*6)=213
213 % 10 = 3
So 99983-26-3 is a valid CAS Registry Number.
99983-26-3Relevant academic research and scientific papers
PROCESS FOR PREPARING 2-(1-(tert-BUTOXYCARBONYL)PIPERIDINE-4-YL)BENZOIC ACID
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, (2019/12/15)
The invention relates to processes for preparing 2-(1-(tert-butoxycarbonyl)-piperidine-4-yl)benzoic acid having formula I: Among its various uses, this compound is useful as an intermediate for preparing ampreloxetine and salts thereof.
Syntheses and in vitro evaluation of decalinvesamicol analogues as potential imaging probes for vesicular acetylcholine transporter (VAChT)
Kozaka, Takashi,Uno, Izumi,Kitamura, Yoji,Miwa, Daisuke,Ogawa, Kazuma,Shiba, Kazuhiro
, p. 4936 - 4941 (2012/10/08)
A series of vesamicol analogues, o-iodo-trans-decalinvesamicol (OIDV) or o-bromo-trans-decalinvesamicol (OBDV), were synthesized and their affinities to vesicular acetylcholine transporter (VAChT) and σ receptors (σ-1, σ-2) were evaluated by in vitro bind
