6597-42-8 Usage
Explanation
The compound is composed of 19 carbon (C), 19 hydrogen (H), 1 nitrogen (N), and 1 oxygen (O) atoms.
Explanation
The compound has a solid state and exhibits a color ranging from yellow to light brown.
Explanation
It is utilized as a reagent in the synthesis of various organic compounds and is also used for research purposes in the field of chemistry.
Explanation
The compound is derived from a ketone, which is a carbonyl compound with a C=O double bond.
Explanation
The compound has a phenyl group (C6H5) attached to its structure, which is a characteristic feature of aromatic compounds.
Explanation
The compound may possess biological activity, which means it could interact with living organisms or biological systems, although the specific activity is not mentioned.
Explanation
The compound is considered to have a wide range of potential applications in various fields of science and industry due to its unique structure and properties.
Explanation
The specific properties and uses of the compound may vary depending on the particular application it is intended for, highlighting its adaptability in different contexts.
Appearance
Yellow to light brown solid
Usage
Organic synthesis and research
Chemical Classification
Ketone derivative
Substitution
Substituted phenyl group
Biological Activity
Potential
Versatility
Versatile chemical reagent
Application
Depends on precise application
Check Digit Verification of cas no
The CAS Registry Mumber 6597-42-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,9 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6597-42:
(6*6)+(5*5)+(4*9)+(3*7)+(2*4)+(1*2)=128
128 % 10 = 8
So 6597-42-8 is a valid CAS Registry Number.
6597-42-8Relevant academic research and scientific papers
Characterization of the Fluorescence Properties of 4-Dialkylaminochalcones and Investigation of the Cytotoxic Mechanism of Chalcones
Zhou, Bo,Jiang, Peixin,Lu, Junxuan,Xing, Chengguo
, p. 539 - 552 (2016/08/26)
Understanding the mechanisms responsible for the various biological activities of chalcones, particularly the direct cellular targets, presents an unmet challenge. Here, we prepared a series of fluorescent chalcone derivatives as chemical probes for their
Synthesis and structure-affinity relationships of novel dibenzylideneacetone derivatives as probes for ?-Amyloid Plaques
Cui, Mengchao,Ono, Masahiro,Kimura, Hiroyuki,Liu, Boli,Saji, Hideo
, p. 2225 - 2240 (2011/06/17)
A new and extensive set of dibenzylideneacetone derivatives was synthesized and screened for affinity toward A1-42 aggregates. Structure-activity relationships revealed the binding of dibenzylideneacetones to be affected by various substituents. The introduction of a substituent group in the ortho position reduced or abolished the binding. However, the para position was highly tolerant of sterically demanding substitutions. Three radioiodinated ligands (6, 70, and 71) and two 18F fluoro-pegylated (FPEG) ligands (83 and 85) were prepared, all of which displayed high affinity for A1-42 aggregates (Ki ranging from 0.9 to 7.0 nM). In biodistribution experiments, they exhibited good initial penetration (1.59, 4.68, 4.56, 4.13, and 5.15% ID/g, respectively, at 2 min) of and fast clearance from the brain. Autoradiography with sections of postmortem AD brain and transgenic mouse brain confirmed the high affinity of these tracers. These preliminary results strongly suggest the dibenzylideneacetone structure to be a potential new scaffold for β-amyloid imaging probes.
