79784-62-6 Usage
Uses
Used in Pharmaceutical Synthesis:
4-pentanoylbenzoic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex organic molecules. Its presence in the molecular structure of certain drugs can contribute to their therapeutic effects and pharmacological properties.
Used in Organic Compound Production:
In the chemical industry, 4-pentanoylbenzoic acid is used as a building block for the production of other organic compounds. Its versatile structure allows for the creation of a wide range of chemical entities, which can be tailored for specific applications.
Used in Research and Development:
4-pentanoylbenzoic acid is utilized in research and development settings to explore its potential applications and to understand its chemical behavior. This can lead to the discovery of new uses and the optimization of existing processes involving 4-pentanoylbenzoic acid.
Used in Drug Delivery Systems:
Although not explicitly mentioned in the provided materials, given its role in pharmaceutical synthesis, 4-pentanoylbenzoic acid could potentially be used in the development of drug delivery systems to improve the bioavailability and efficacy of certain medications.
Check Digit Verification of cas no
The CAS Registry Mumber 79784-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,8 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79784-62:
(7*7)+(6*9)+(5*7)+(4*8)+(3*4)+(2*6)+(1*2)=196
196 % 10 = 6
So 79784-62-6 is a valid CAS Registry Number.
79784-62-6Relevant articles and documents
Deactivation of Triplet Phenyl Alkyl Ketones by Conjugatively Electron-Withdrawing Substituents
Wagner, Peter J.,Siebert, Elizabeth J.
, p. 7329 - 7335 (2007/10/02)
Para-cyano, -carbomethoxy, and -acyl substituents decrease the triplet reactivity of valerophenone (γ-hydrogen abstraction), whereas comparable meta substituents increase reactivity.Spectroscopic results are presented which indicate that para-(-R) substituents lower ?,?* triplet energies so much more than n,?* energies that the lowest triplets become largely ?,?* in nature.Meta-(-R) substituents do not stabilize ?,?* triplets enough to invert triplet levels.Both substitution patterns support a largely 1,4-biradical structure for the lowest ?,?* triplet of acylbenzenes.Ortho substituents show the usual steric anomalies: ortho cyano enhances valerophenone triplet reactivity by stabilizing the n,?* triplet; ortho carbomethoxy deactivates valerophenone by stabilizing the ?,?* triplet but not the n,?.*
