40943-25-7 Usage
Uses
Used in Pharmaceutical Industry:
2-CHLORO-1-(4-HYDROXY-3,5-DIMETHYLPHENYL)-1-ETHANONE is used as a chemical intermediate for the synthesis of therapeutic agents and biologically active compounds. Its unique structure allows for the development of new drugs with potential applications in treating various diseases and medical conditions.
Used in Research Applications:
In research settings, 2-CHLORO-1-(4-HYDROXY-3,5-DIMETHYLPHENYL)-1-ETHANONE serves as a valuable compound for studying the properties and mechanisms of action of related chemical compounds. It can provide insights into the design and development of novel pharmaceuticals and other bioactive substances.
Used as a Reagent in Organic Synthesis:
2-CHLORO-1-(4-HYDROXY-3,5-DIMETHYLPHENYL)-1-ETHANONE is used as a reagent in organic synthesis to introduce a chloro group into other molecules. This property makes it a useful tool for the modification of existing compounds and the creation of new chemical entities with desired properties.
Safety Considerations:
2-CHLORO-1-(4-HYDROXY-3,5-DIMETHYLPHENYL)-1-ETHANONE can be hazardous if not handled and stored properly. It should be used in a controlled laboratory setting by trained professionals who follow safety guidelines to ensure the safe handling and disposal of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 40943-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,4 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40943-25:
(7*4)+(6*0)+(5*9)+(4*4)+(3*3)+(2*2)+(1*5)=107
107 % 10 = 7
So 40943-25-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO2/c1-6-3-8(9(12)5-11)4-7(2)10(6)13/h3-4,13H,5H2,1-2H3
40943-25-7Relevant academic research and scientific papers
A facile halogen exchange of active methylene chloro compounds
Bhalerao, U. T.,Raju, B. Chinna,Neelakantan, Parvathi
, p. 1197 - 1199 (2007/10/02)
An unexpected exchange of chlorine with bromine occurs during benzylation of 2-chloro-4'-hydroxy-3',5'-dimethylacetophenone (1a) with benzyl bromide.The products (2, 3 and 4) formed constitute a 60:40 mixture of chloro and bromo derivatives.A simple methodology for such an exchange in two-phase system with aq.HBr in the presence of phase transfer catalyst (PTC) is described.