2-[(6-Hydroxy[1,1'-biphenyl]-3-yl)carbonyl]benzoic acid compd. with 1-[2-[(S)-(4-chlorophenyl)phenylmethoxy]ethyl]piperidine

Base Information

Chemical Name:2-[(6-Hydroxy[1,1'-biphenyl]-3-yl)carbonyl]benzoic acid compd. with 1-[2-[(S)-(4-chlorophenyl)phenylmethoxy]ethyl]piperidine
CAS No.:220329-19-1
Molecular Formula:C40H38ClNO5
Molecular Weight:648.18642
Hs Code.:
Mol file:220329-19-1.mol

Synonyms:Levocloperastine Fendizoic Acid Salt

Suppliers and Price of 2-[(6-Hydroxy[1,1'-biphenyl]-3-yl)carbonyl]benzoic acid compd. with 1-[2-[(S)-(4-chlorophenyl)phenylmethoxy]ethyl]piperidine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(S)-CloperastineFendizoate
10mg
$ 205.00

Total 69 raw suppliers

Chemical Property of 2-[(6-Hydroxy[1,1'-biphenyl]-3-yl)carbonyl]benzoic acid compd. with 1-[2-[(S)-(4-chlorophenyl)phenylmethoxy]ethyl]piperidine

Chemical Property:

PSA：87.07000
LogP:8.85820

Purity/Quality:

99%, ^*data from raw suppliers

(S)-CloperastineFendizoate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses non-steroidal anti-inflammatory (S)-Cloperastine Fendizoate is the salt of (S)-Cloperastine (C587195), used in the treatment of chronic non-productive cough. Antitussive.

Technology Process of 2-[(6-Hydroxy[1,1'-biphenyl]-3-yl)carbonyl]benzoic acid compd. with 1-[2-[(S)-(4-chlorophenyl)phenylmethoxy]ethyl]piperidine

There total 3 articles about 2-[(6-Hydroxy[1,1'-biphenyl]-3-yl)carbonyl]benzoic acid compd. with 1-[2-[(S)-(4-chlorophenyl)phenylmethoxy]ethyl]piperidine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.2%

: 3703-76-2,132301-89-4
Cloperastine

: 84627-04-3
2-<(2'-hydroxy-5'-biphenylyl)carbonyl>benzoic acid

: 220329-19-1
levocloperastine fendizoate

Guidance literature:: In water; acetone; for 2h; Solvent; Reflux;

Reference yield:

: 119-56-2
(4-chlorophenyl)phenylmethanol

: 220329-19-1
levocloperastine fendizoate

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuric acid / toluene / 5 h / Reflux

2: sodium carbonate / 14 h / 95 °C

3: acetone; water / 2 h / Reflux

With sulfuric acid; sodium carbonate; In water; acetone; toluene;

Reference yield:

: 5321-46-0,132301-88-3
(4-chlorophenyl)phenylmethyl 2-chloroethyl ether

: 220329-19-1
levocloperastine fendizoate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium carbonate / 14 h / 95 °C

2: acetone; water / 2 h / Reflux

With sodium carbonate; In water; acetone;