81574-72-3 Usage
Explanation
Different sources of media describe the Explanation of 81574-72-3 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. These are the specific atoms or groups of atoms that are attached to the benzene ring, giving the compound its unique chemical properties.
3. The compound is derived from a phenol (a hydroxyl group attached to a benzene ring) with additional substituents (bromine, chlorine, and methoxy groups) attached to the ring.
4. The presence of multiple functional groups allows the compound to participate in various chemical reactions, making it a useful building block for the synthesis of other organic compounds.
5. Due to its reactivity and the presence of multiple functional groups, 1-bromo-2-chloro-3,5-dimethoxybenzene is used in the synthesis of pharmaceuticals and organic compounds, as well as in research and development of new drugs.
6. The compound can undergo these types of reactions, which involve the replacement of one atom or group with another, making it a valuable reagent in organic chemistry.
7. Most organic compounds with molecular weights similar to 1-bromo-2-chloro-3,5-dimethoxybenzene are solids or liquids at room temperature, although the exact physical state may depend on specific conditions.
8. The compound is likely to be soluble in organic solvents such as dichloromethane, ethyl acetate, or acetone, due to its nonpolar nature and the presence of the benzene ring.
9. As with many organic compounds, 1-bromo-2-chloro-3,5-dimethoxybenzene may pose health risks if not handled properly, such as being an irritant or toxic if ingested, inhaled, or absorbed through the skin.
10. To maintain the stability and safety of the compound, it should be stored in a cool, dry, and well-ventilated area, away from heat, moisture, and direct sunlight.
Functional groups
Bromine, chlorine, and methoxy groups
Structure
Substituted phenol derivative
Reactivity
Versatile and reactive
Applications
Pharmaceutical synthesis, organic chemistry, medicinal chemistry, and drug development
Reaction types
Nucleophilic substitution and aromatic substitution
Physical state
Likely a solid or liquid at room temperature
Solubility
Soluble in organic solvents
Hazards
Potential irritant or toxic
Storage
Store in a cool, dry, and well-ventilated area
Check Digit Verification of cas no
The CAS Registry Mumber 81574-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,7 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81574-72:
(7*8)+(6*1)+(5*5)+(4*7)+(3*4)+(2*7)+(1*2)=143
143 % 10 = 3
So 81574-72-3 is a valid CAS Registry Number.
81574-72-3Relevant articles and documents
FGFR INHIBITOR AND APPLICATION THEREOF
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Paragraph 0102-0103, (2020/01/22)
An azatricyclic compound (as represented by formula I) which acts as an inhibitor of fibroblast growth factor receptors (FGFR), as well as a pharmaceutical composition thereof, a preparation method, and a use therefor in the treatment of FGFR-mediated diseases. The azatricyclic compound exerts an effect by means of participating in the regulation of a plurality of processes such as cell proliferation, apoptosis, migration, neovascularization, and the like. AA%%%Formula (I).
Depsidone Synthesis. Part 21. A New Synthesis of Grisa-2',5'-diene-3,4'-diones
Sargent, Melvyn V.
, p. 403 - 411 (2007/10/02)
Treatment of suitably substituted methyl 2-phenoxybenzoates with titanium(IV) chloride and dry hydrogen chloride afforded grisa-2',5'-diene-3,4'-diones in high yield.The structures of these compounds followed from their thermal stability, their methanolysis to methyl 2-(4-hydroxyphenoxy)benzoates, and their reductive cleavage to 2,4'-dihydrobenzophenones.Treatment of the benzophenones with base gave xanthones.An attempt to synthesize dehydrogriseofulvin (1) by this method failed.
