5365-79-7 Usage
Chemical structure
1-bromononadecan-2-one consists of a nonadecane chain with a ketone functional group at the second carbon atom and a bromine atom at the first carbon atom.
Functional groups
The compound has a ketone functional group (C=O) and a bromine atom (Br).
Synthesis
It can be produced by the reaction of nonadecane with bromine and aluminum chloride.
Synthetic intermediate
Used in the synthesis of various organic compounds.
Reagent
Utilized in chemical reactions, such as nucleophilic substitution reactions.
Pharmaceutical industry
Potential applications due to its versatile chemical structure.
Agrochemical industry
Potential applications in the development of new agrochemicals.
Physical properties
The specific physical properties of 1-bromononadecan-2-one are not provided in the material, but it is likely a liquid or solid at room temperature, given its long hydrocarbon chain.
Reactivity
The compound is likely to undergo nucleophilic substitution reactions due to the presence of the bromine atom.
Solubility
It may be soluble in organic solvents, such as dichloromethane or ethyl acetate, due to its nonpolar nature.
Safety
The safety information for 1-bromononadecan-2-one is not provided in the material, but it is important to consider the potential hazards associated with bromine-containing compounds, such as toxicity and environmental impact.
Check Digit Verification of cas no
The CAS Registry Mumber 5365-79-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5365-79:
(6*5)+(5*3)+(4*6)+(3*5)+(2*7)+(1*9)=107
107 % 10 = 7
So 5365-79-7 is a valid CAS Registry Number.
5365-79-7Relevant academic research and scientific papers
Synthesis and antibiofilm activity of a second-generation reverse-amide oroidin library: A structure-activity relationship study
Eric Ballard,Richards, Justin J.,Wolfe, Amanda L.,Melander, Christian
experimental part, p. 10745 - 10761 (2009/12/04)
A second-generation library of 2-aminoimidazole-based derivatives incorporating a "reversed amide" (RA) motif in comparison to the marine natural product oroidin were synthesized and subsequently assayed for antibiofilm activity against the medically relevant Gram-negative proteobacteria P. aeruginosa and A. baumannii. Most notably, an in-depth activity profile is reported for the most active subclass of derivatives that bear linear aliphatic chains off the amide bond. Additionally, further structural modifications of the core template, such as removal of the amide bond or substitution with a triazole isostere, resulted in the discovery of analogues with antibiofilm activities that varied with respect to their inhibition and dispersal properties of P. aeruginosa and A. baumannii biofilms.
SYNTHESIS OF TETRATHIAFULVALENES WITH LONG-CHAIN SUBSTITUENTS
Kreitsberga, Ya. N.,Bite, D. V.,Kampar, V. E.,Kampare, R. B.,Neiland, O. Ya.
, p. 931 - 937 (2007/10/02)
Tetrathiafulvalenes with long-chain alkyl substituents (C17H35 an C16H33) were obtained by a many-stage synthesis from 1-diazo-2-nonadecanone, 1-diazooctadecane, or 18-pentatriacontanone.Their structures were confirmed by their IR, electronic, and PMR spectra.Their ionization potentials were determined.
