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1-(3-fluorobenzyl)pyridin-1-ium bromide is a chemical compound with the molecular formula C12H10BrFN. It is a derivative of pyridinium, a heterocyclic compound with a nitrogen atom in the ring structure. The compound features a 3-fluorobenzyl group attached to the pyridine ring, which introduces a fluorine atom at the meta position of the benzene ring. The bromide ion is present as a counterion, making it a salt. 1-(3-fluorobenzyl)pyridin-1-ium bromide is often used in organic synthesis and as an intermediate in the preparation of various pharmaceuticals and agrochemicals. Its unique structure with a fluorine atom and a pyridine ring provides it with specific reactivity and properties that can be exploited in chemical reactions.

330-49-4

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330-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 330-49-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 330-49:
(5*3)+(4*3)+(3*0)+(2*4)+(1*9)=44
44 % 10 = 4
So 330-49-4 is a valid CAS Registry Number.

330-49-4Downstream Products

330-49-4Relevant academic research and scientific papers

Application of primary halogenated hydrocarbons for the synthesis of 3-Aryl and 3-Alkyl indolizines

Liu, Yan,Hu, Huayou,Zhou, Junyu,Wang, Wenhui,He, Youliang,Wang, Chao

, p. 5016 - 5024 (2017)

Indolizine is an important heterocyclic compound with several interesting properties that make it suitable for numerous applications in many fields, such as biology, medicine and materials. However, the synthesis of 3-Alkyl indolizines from bulky primary halogenated alkanes has not yet been reported. Herein, a transition-metal-free synthetic route to 3-Aryl and 3-Alkyl indolizines from electron-deficient alkenes, pyridines and primary halogenated hydrocarbons has been reported for the first time using a tandem reaction. The key step of this method is the oxidative dehydrogenative aromatization of a tetrahydroindolizine intermediate with 2,2,6,6-Tetramethylpiperidine-N-oxyl (TEMPO) as the oxidant. The advantages of this protocol are its use of easily available and low-cost starting materials, the transition-metal-free conditions and its ready scalability.

Fluorinated Boronic Acid-Appended Pyridinium Salts and 19F NMR Spectroscopy for Diol Sensing

Axthelm, J?rg,Askes, Sven H. C.,Elstner, Martin,Upendar Reddy,G?rls, Helmar,Bellstedt, Peter,Schiller, Alexander

, p. 11413 - 11420 (2017)

The identification and discrimination of diols is of fundamental importance in medical diagnostics, such as measuring the contents of glucose in the urine of diabetes patients. Diol sensors are often based on fluorophore-appended boronic acids, but these

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