220329-19-1 Usage
Description
2-[(6-Hydroxy[1,1'-biphenyl]-3-yl)carbonyl]benzoic acid compd. with 1-[2-[(S)-(4-chlorophenyl)phenylmethoxy]ethyl]piperidine is a complex organic compound with a unique chemical structure. It is characterized by the presence of a biphenyl group, a carbonyl group, and a piperidine ring, among other functional groups. 2-[(6-Hydroxy[1,1'-biphenyl]-3-yl)carbonyl]benzoic acid compd. with 1-[2-[(S)-(4-chlorophenyl)phenylmethoxy]ethyl]piperidine has potential applications in various fields due to its specific chemical properties and interactions with other molecules.
Uses
Used in Pharmaceutical Industry:
2-[(6-Hydroxy[1,1'-biphenyl]-3-yl)carbonyl]benzoic acid compd. with 1-[2-[(S)-(4-chlorophenyl)phenylmethoxy]ethyl]piperidine is used as a non-steroidal anti-inflammatory agent for the treatment of various inflammation-related conditions. Its chemical structure allows it to inhibit the production of inflammatory mediators, providing relief from pain and swelling.
Used in Antitussive Applications:
In the pharmaceutical industry, 2-[(6-Hydroxy[1,1'-biphenyl]-3-yl)carbonyl]benzoic acid compd. with 1-[2-[(S)-(4-chlorophenyl)phenylmethoxy]ethyl]piperidine is also used as an antitussive agent. It is the salt of (S)-Cloperastine (C587195) and is specifically used in the treatment of chronic non-productive cough. The compound works by suppressing the cough reflex, providing relief from persistent coughing.
Different applications in different industries may include:
Used in Chemical Industry:
2-[(6-Hydroxy[1,1'-biphenyl]-3-yl)carbonyl]benzoic acid compd. with 1-[2-[(S)-(4-chlorophenyl)phenylmethoxy]ethyl]piperidine could be used as an intermediate in the synthesis of other complex organic compounds, such as pharmaceuticals, agrochemicals, or specialty chemicals. Its unique structure and functional groups make it a valuable building block for creating novel molecules with specific properties and applications.
Used in Research and Development:
2-[(6-Hydroxy[1,1'-biphenyl]-3-yl)carbonyl]benzoic acid compd. with 1-[2-[(S)-(4-chlorophenyl)phenylmethoxy]ethyl]piperidine may also be utilized in research and development settings to study its interactions with various biological targets, such as enzymes, receptors, or ion channels. Understanding these interactions can lead to the discovery of new therapeutic agents or provide insights into the mechanisms of existing drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 220329-19-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,3,2 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 220329-19:
(8*2)+(7*2)+(6*0)+(5*3)+(4*2)+(3*9)+(2*1)+(1*9)=91
91 % 10 = 1
So 220329-19-1 is a valid CAS Registry Number.
220329-19-1Relevant articles and documents
A left hand chlorine paipai Si Tingfenoak acid preparation method of the
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Paragraph 0143; 0144; 0161; 0172; 0187; 0202, (2017/08/25)
The invention discloses a preparation method of levo cloperastine fendizoate, which comprises the following steps: carrying out nucleophilic substitution reaction on 4-chlorobenzhydrol and 2-chloroethanol in a benzene organic solvent, so that an intermediate product is obtained; reacting the intermediate product with piperidine, so that racemic cloperastine is obtained; resolving the racemic cloperastine by using a resolving agent in a fatty alcohol solvent, so that levo cloperastine is obtained; and carrying out salt forming reaction on the levo cloperastine and a fendizoic acid, so that levo cloperastine fendizoate is obtained, wherein the resolving agent is an R-substituted dibenzoyl-L-tartaric acid, and R refers to alkyl, alkoxy, -Cl, -F, -Br or -H. In the method provided by the invention, in a fatty alcohol solvent, an R-substituted dibenzoyl-L-tartaric acid is adopted as a resolving agent for carrying out resolving on racemic cloperastine, and the resolving yield is high, so that the obtained levo cloperastine fendizoate has high optical purity, and has a high product yield.
