945543-21-5 Usage
Description
(2-chloro-6-iodophenyl)methanol, with the molecular formula C7H6ClIO, is a chemical compound that serves as a versatile building block in organic synthesis. It is characterized by the presence of a chlorine atom at the 2nd position and an iodine atom at the 6th position on a phenyl ring, with a methanol group attached to the benzylic carbon. This unique structure endows it with properties that make it a valuable reagent in the preparation of various biologically active compounds and pharmaceuticals.
Uses
Used in Pharmaceutical Development:
(2-chloro-6-iodophenyl)methanol is used as an intermediate in the synthesis of potential anticancer agents and antifungal drugs. Its unique structure allows for the development of new compounds with improved therapeutic properties and efficacy against a range of diseases.
Used in Organic Synthesis:
As a reagent, (2-chloro-6-iodophenyl)methanol is utilized in the preparation of various biologically active compounds. Its versatility in organic synthesis makes it a valuable tool for creating new molecules with potential applications in medicine and other fields.
Used in Material Science:
(2-chloro-6-iodophenyl)methanol is also known for its use in the development of new materials. Its unique chemical properties can contribute to the creation of innovative materials with specific characteristics, such as improved stability or reactivity.
Used in Agrochemical Production:
In the agrochemical industry, (2-chloro-6-iodophenyl)methanol is used in the production of various chemicals that are employed in agriculture. Its role in this sector highlights its broad applicability and the potential for further development of agrochemicals with enhanced performance.
Due to its diverse range of applications, (2-chloro-6-iodophenyl)methanol is of significant interest to researchers in the fields of organic chemistry and pharmaceutical development, as it offers a foundation for the creation of new and improved compounds with potential benefits across multiple industries.
Check Digit Verification of cas no
The CAS Registry Mumber 945543-21-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,5,4 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 945543-21:
(8*9)+(7*4)+(6*5)+(5*5)+(4*4)+(3*3)+(2*2)+(1*1)=185
185 % 10 = 5
So 945543-21-5 is a valid CAS Registry Number.
945543-21-5Relevant articles and documents
Stereoretentive Intramolecular Glycosyl Cross-Coupling: Development, Scope, and Kinetic Isotope Effect Study
Yi, Duk,Zhu, Feng,Walczak, Maciej A.
, p. 4627 - 4631 (2018)
A series of cyclic C-glycosides were synthesized using the palladium-catalyzed stereoretentive intramolecular glycosylation of aryl iodides by employing a bulky phosphine ligand. A variety of functional groups are tolerated in the reaction, and enantioenr
Palladium-Catalyzed, Norbornene-Mediated, ortho-Amination ipso-Amidation: Sequential C-N Bond Formation
Whyte, Andrew,Olson, Maxwell E.,Lautens, Mark
supporting information, p. 345 - 348 (2018/01/27)
A palladium-catalyzed, norbornene-mediated ortho- and ipso-C-N bond-forming Catellani reaction is reported. This reaction proceeds through a sequential intermolecular amination followed by intramolecular cyclization of a tethered amide. The products, ortho-aminated dihydroquinolinones, were generated in moderate to good yields and are present in bioactive molecules. This work highlights the challenge of competing intra- vs intermolecular palladium-catalyzed processes.
