23167-99-9 Usage
Description
2,4-dipropylphenol, commonly known as propofol, is a chemical compound that serves as a general anesthetic. It is a clear, colorless liquid administered intravenously, characterized by its rapid onset and short duration of action. Propofol is renowned for its effectiveness in inducing and maintaining anesthesia during surgical procedures, working by enhancing the activity of gamma-aminobutyric acid (GABA) receptors in the brain, which leads to sedation and unconsciousness.
Uses
Used in Medical and Surgical Procedures:
2,4-dipropylphenol is used as a general anesthetic for inducing and maintaining unconsciousness during surgical operations. It is favored for its quick onset and brief action duration, making it suitable for both pediatric and adult patients.
Used in Anesthesia:
In the field of anesthesia, 2,4-dipropylphenol is utilized as a key component to ensure sedation and amnesia during medical procedures that require a controlled state of unconsciousness.
However, it is important to note that the use of 2,4-dipropylphenol comes with potential side effects such as respiratory depression, hypotension, and the risk of addiction or abuse, which must be carefully managed by medical professionals.
Check Digit Verification of cas no
The CAS Registry Mumber 23167-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,6 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 23167-99:
(7*2)+(6*3)+(5*1)+(4*6)+(3*7)+(2*9)+(1*9)=109
109 % 10 = 9
So 23167-99-9 is a valid CAS Registry Number.
23167-99-9Relevant articles and documents
XH-14 analogues as adenosine antagonists
Scammells, Peter J.,Baker, Stephen P.,Beauglehole, Anthony R.
, p. 1517 - 1524 (2007/10/03)
Analogues of the potent adenosine antagonist 5-(3'-hydroxypropyl)-7-methoxy-2-(3'-methoxy-4'-hydroxyphenyl)benzo[b]furan-3-carbaldehyde (XH-14, 1) with alternate substituents in the 2-, 5- and 7-positions have been synthesised. The affinity of these compo
Alumina-Catalyzed Reactions of Hydroxyarenes and Hydroaromatic Ketones. 9. Reaction of Phenol with 1-Propanol
Klemm, LeRoy H.,Taylor, Dennis R.
, p. 4320 - 4326 (2007/10/02)
At 250-350 deg C in the presence of alumina, phenol (1) reacts with excess 1-propanol to give mainly (>90percent) C-alkylation to form mono- to penta-n-propylphenols plus some O-alkylations to form n-propyl aryl ethers. The principal component of the product mixture from 1 is 2,6-di-n-propylphenol (26-50 mol percent yield). With 4-n-propylphenol as substrate (instead of 1), tri-, tetra-, and penta-n-propylphenols are formed in 48-79percent combined yield. On the average, only 3percent of the total C3H7 groups in the product mixture are isopropyl ones. Deoxygenation is not observed. It is proposed that the principal products result from an SN2-type reaction mechanism which involves nucleophilic attack (variously by C-2, C-4, C-6, or O) of an adsorbed ambident phenoxide ion onto C-1 of an adsorbed n-propoxide group. n-Propylation at C-3 and C-5 of the phenol ring results from surface-catalyzed dienone-phenol rearrangement.Isopropylation may occur via a side reaction of SN1 type.
