111479-09-5 Usage
Description
2-(4-methoxyphenoxy)propanoyl chloride is a chemical compound that features a propanoyl chloride group connected to a 4-methoxyphenoxy moiety. It is recognized for its role as a versatile acylation reagent in organic synthesis, participating in reactions such as acylation and nucleophilic substitution. 2-(4-methoxyphenoxy)propanoyl chloride is also valued for its utility as an intermediate in the creation of pharmaceuticals and agrochemicals, as well as for its potential as a building block in polymer and high-performance material production.
Uses
Used in Pharmaceutical Synthesis:
2-(4-methoxyphenoxy)propanoyl chloride is used as an intermediate for the synthesis of pharmaceuticals, leveraging its acylation properties to form complex organic molecules that are integral to the development of new drugs.
Used in Agrochemical Production:
In the agrochemical industry, 2-(4-methoxyphenoxy)propanoyl chloride serves as a key intermediate, contributing to the creation of compounds that are used in the development of pesticides and other agricultural chemicals to enhance crop protection and yield.
Used in Polymer Production:
2-(4-methoxyphenoxy)propanoyl chloride is utilized as a building block in the production of polymers, where its unique structure allows for the formation of polymers with specific properties tailored for various applications.
Used in High-Performance Material Manufacturing:
2-(4-methoxyphenoxy)propanoyl chloride is also used as a component in the manufacturing of high-performance materials, where its reactivity and structural features contribute to the creation of materials with enhanced characteristics for specialized uses.
Overall, 2-(4-methoxyphenoxy)propanoyl chloride is a multifaceted chemical with applications across several industries, underscoring its importance in the realm of organic chemistry and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 111479-09-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,7 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111479-09:
(8*1)+(7*1)+(6*1)+(5*4)+(4*7)+(3*9)+(2*0)+(1*9)=105
105 % 10 = 5
So 111479-09-5 is a valid CAS Registry Number.
111479-09-5Relevant articles and documents
Mutual Kinetic Resolution of Racemic 3,4-Dihydro-3-methyl-2H-[1,4]benzoxazines with Acyl Chlorides of Racemic O-Phenyllactic Acids and DFT Modelling of Transition States
Korolyova, Marina A.,Vakarov, Sergey A.,Kozhevnikov, Dmitry N.,Gruzdev, Dmitry A.,Levit, Galina L.,Krasnov, Victor P.
supporting information, p. 4577 - 4585 (2018/09/06)
The effect of the electronic nature of the para substituent on the aromatic ring of 2-aryloxypropionyl chlorides on the stereochemical outcome of the acylation of 3,4-dihydro-3-methyl-2H-[1,4]benzoxazine and its 7,8-difluoro-containing analogue has been studied. The geometries of the diastereoisomeric transition states and the corresponding Gibbs free enthalpies of activation were determined through DFT calculations at the COSMO-CH2Cl2-B3LYP-D3-gCP/def2-TZVP (or def2-SVP)//B3LYP-D3-gCP/def2-SVP level of theory. It has been found that a low-cost quantum chemical calculation at a chosen level of theory describes well the quantitative dependence of the selectivity of acylation on the structures of the reagents. The obtained results indicate that aromatic interactions between the reagents play a significant role in the process of stereodifferentiation, ensuring high selectivity of the acylation of benzoxazines with 2-aryloxyacyl chlorides.
PRECURSOR COMPOUNDS OF SWEET TASTE RECEPTOR ANTAGONISTS FOR THE PREVENTION OR TREATMENT OF DISEASE
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Page/Page column 21, (2011/04/14)
A description is given of precursor compounds of sweet taste receptor antagonists for the prevention or treatment of disease, in particular for the prevention or treatment of Type 2 diabetes. A description is also given of uses of these precursor compound
