53400-42-3 Usage
Chemical structure
The compound consists of a pentane chain with a ketone group attached to the third carbon and a dimethylamino group attached to the first carbon.
Functional groups
It contains a ketone group (C=O) and a dimethylamino group (N(CH3)2).
Hydrochloride salt form
The compound is in the form of a hydrochloride salt, which allows for easier handling and storage.
Reagent in organic synthesis
It is commonly used as a reagent in organic synthesis, particularly in the preparation of pharmaceuticals and other useful compounds.
Versatile building block
Its precise chemical structure makes it a versatile building block for the synthesis of a wide range of complex molecules.
Research and industry applications
Its use in research and industry continues to expand due to its versatility and the ease of handling the hydrochloride salt form.
Solubility
The hydrochloride salt form is likely to be more soluble in water compared to the free base form, which can be advantageous for certain applications.
Stability
The hydrochloride salt form may offer improved stability compared to the free base form, making it a more convenient option for laboratories.
Polarity
The presence of the dimethylamino group and the hydrochloride salt form may result in increased polarity compared to other similar compounds without these functional groups.
Potential reactivity
The compound may react with strong acids, strong bases, or other nucleophiles due to the presence of the ketone and dimethylamino groups.
Check Digit Verification of cas no
The CAS Registry Mumber 53400-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,0 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53400-42:
(7*5)+(6*3)+(5*4)+(4*0)+(3*0)+(2*4)+(1*2)=83
83 % 10 = 3
So 53400-42-3 is a valid CAS Registry Number.
53400-42-3Relevant academic research and scientific papers
Synthesis and plant-growth regulatory activities of novel imine derivatives containing 1H-1,2,4-triazole and thiazole rings
Qin, Xue,Yu, Hai Bo,Dai, Hong,Qin, Zhen Fang,Zhang, Xin,Bing, Gui Fang,Wang, Ting Ting,Fang, Jian Xin
scheme or table, p. 283 - 286 (2010/12/19)
Eleven new imine derivatives 6 containing 1H-1,2,4-triazole and thiazole rings were synthesized by the condensation of 5-((1H-1,2,4-triazol-1-yl)methyl)-4-tert-butylthiazol-2-amine with various substituted benzaldehydes. The structures of the title compounds were characterized by 1H NMR, MS and elemental analysis. The plant-growth regulatory activities of these compounds were evaluated. The primary bioassay results indicated that these target compounds exhibited promising plant-growth regulatory activities.
Efficient Preparation of Substituted 5,6,7,8-Tetrahydroquinolines and Octahydroacridine Derivatives
Sielemann, Dirk,Keuper, Ralf,Risch, Nikolaus
, p. 487 - 491 (2007/10/03)
The reaction of the enamine 4 with different β-amino ketone hydrochlorides 3a-e affords the diketones 5a-e which can be cyclized to the corresponding mono- and disubstituted tetrahydroquinolines 6a-e. Furthermore the preparation of the octahydroacridines 8f and 8g by using a straightforward multi step sequence is described.
DESTRUCTIVE NITRATION OF POLYNITRO CARBONYL COMPOUNDS I. A NEW METHOD FOR THE PRODUCTION OF HEXANITROETHANE
Golod, E. L.,Bagal, L. I.
, p. 29 - 33 (2007/10/02)
The nitration of 1,1,1-trinitroalkyl ketones (NO2)3C(CH2)nCOR with a mixture of concentrated nitric and sulfuric acids leads to the formation of hexanitroethane with a yield of up to 80percent.The reaction is promoted by electron-donating substituents. 1,1-Dinitro-4-pentanone is nitrated in a similar way.Hexanitroethane is not formed in nitric acid alone.
