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Uniprofen

CAS No.
51234-28-7
Chemical Name:
Uniprofen
Synonyms
Opren;Coxigon;Oraflex;Inflamid;LY-90459;Uniprofen;LRCL-3794;NSC 299582;Aids128826;Lilly-90459
CBNumber:
CB0875361
Molecular Formula:
C16H12ClNO3
Molecular Weight:
301.73
MDL Number:
MOL File:
51234-28-7.mol
MSDS File:
SDS
Last updated:2023-09-04 15:51:00

Uniprofen Properties

Melting point 189.5°C
Boiling point 446.2±30.0 °C(Predicted)
Density 1.2411 (rough estimate)
refractive index 1.6470 (estimate)
storage temp. Refrigerator
solubility DMSO: slightly; Methanol: slightly, sonicated
form A solid
pka 4.36±0.30(Predicted)
color Cream solid from EtOH
FDA UNII 17SZX404IM

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302;H315;H319;H335
Precautionary statements  P261;P305+P351+P338
Toxicity LD50 oral in rat: 118mg/kg
NFPA 704
0
2 0

Uniprofen price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B165300 Benoxaprofen 51234-28-7 10mg $470 2021-12-16 Buy
American Custom Chemicals Corporation API0007668 BENOXAPROFEN 95.00% 51234-28-7 10MG $1045.28 2021-12-16 Buy
American Custom Chemicals Corporation API0007668 BENOXAPROFEN 95.00% 51234-28-7 100MG $4331.25 2021-12-16 Buy
American Custom Chemicals Corporation API0007668 BENOXAPROFEN 95.00% 51234-28-7 1MG $329.7 2021-12-16 Buy
Product number Packaging Price Buy
B165300 10mg $470 Buy
API0007668 10MG $1045.28 Buy
API0007668 100MG $4331.25 Buy
API0007668 1MG $329.7 Buy

Uniprofen Chemical Properties,Uses,Production

Originator

Opren,Dista Lilly,UK,1980

Uses

A non-steroidal anti-inflammatory ophthalmic agent.

Definition

ChEBI: A monocarboxylic acid that is propionic acid substituted at position 2 by a 2-(4-chlorophenyl)-1,3-benzoxazol-5-yl group. It was used as a non-steroidal anti-inflammatory drug until 1982 when it was withdrawn from the market due to adverse side-effects inc uding liver necrosis, photosensitivity, and carcinogenicity in animals.

Manufacturing Process

The 6-benzoxazolyl analog of the 5-benzoxazolyl product is prepared as follows:
(a) Ethyl 2-(2-p-chlorophenyl-6-benzoxazolyl)propionate: A solution of ethyl 2-(3-hydroxy-4-aminophenyl)propionate (2.5 g) in pyridine (15 ml) was treated with p-chlorobenzoyl chloride (1.65 ml) at 5°C. After stirring for 2 hours at room temperature the solution was evaporated to dryness.
The residue was heated at 220°C until no more water was evolved, then was allowed to cool. This yielded ethyl 2-(2-p-Chlorophenyl-6- benzoxazolyl)propionate.
(b) 2-(2-p-Chlorophenyl-6-benzoxazolyl)propionic acid: A solution of ethyl 2- (2-chlorophenyl-6-benzoxazolyl)propionate (4 g) in aqueous sodium hydroxide (30 ml) was heated on a steam bath for one-half hour. On cooling the black solution was washed with chloroform. On acidification of the black solution with hydrochloric acid the mixture was extracted with chloroform. This solution on evaporation yielded 2-(2-p-chlorophenyl-6-benzoxazolyl)propionic acid, MP 196°C.

brand name

Oraflex (Lilly);90459 compound;Benoxapran;Bexopron;Compound 90459;Lilly 3794;Lilly 90459;Lrcl 3794;Oprenal.

Therapeutic Function

Antiinflammatory, Analgesic

World Health Organization (WHO)

Benoxaprofen, a nonsteroidal antiinflammatory agent, was introduced in 1980 for the treatment of rheumatic disorders. Following reports of serious adverse effects, some of which were fatal, it was withdrawn in several countries prior to worldwide withdrawal by the manufacturer in 1982.

Safety Profile

Poison by ingestion, subcutaneous, and intraperitoneal routes. Moderately toxic to humans by ingestion.Human systemic effects by ingestion: jaundice and gynecomastia (excessive development of the male mammary glands), changes in kidney tubules, decreased

28694-90-8
51234-28-7
Synthesis of Uniprofen from 2-(4-aminophenyl)propiononitrile

Uniprofen Suppliers

Global( 39)Suppliers
Supplier Tel Email Country ProdList Advantage
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49390 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Alfa Chemistry
+1-5166625404 Info@alfa-chemistry.com United States 21317 58
Hunan Jibang Biological Technology Co., LTD
+8613776644403 sales02@kingboomtech.com China 1806 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923 1026@dideu.com China 9116 58
Coresyn Pharmatech Co., Ltd.
+86-571-86626709 +86-18157142896 cbc@coresyn.com China 9991 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43348 58
Jilin Chinese Academy of Sciences-yanshen Technology
+undefined18143011203 info@chemextension.com China 42057 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58
J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76

Uniprofen Spectrum

51234-28-7(Uniprofen)Related Search:

Coxigon Opren Oraflex Uniprofen 2-(2-(4-chlorophenyl)benzo[d]oxazol-5-yl)propanoic acid 2-[2-(4-Chlorophenyl)benzoxazol-5-yl]-propanoic Acid dl-Benoxaprofen NSC 299582 2-(4-Chlorophenyl)-α-methyl-5-benzoxazoleacetic acid Compound-90459 Lilly-90459 LRCL-3794 2-(2-(4-Chlorophenyl)-1,3-benzoxazol-5-yl)propanoic acid 2-(p-Chlorophenyl)-.alpha.-methyl-5-benzoxazoleacetic acid 5-Benzoxazoleacetic acid, 2-(4-chlorophenyl)-.alpha.-methyl- Aids128826 Aids-128826 Inflamid 2-(4-Chlorophenyl)-alpha-methyl-5-benzoxazoleacetic acid 5-Benzoxazoleacetic acid, 2-(4-chlorophenyl)-α-methyl- Benoxaphen. Compound 90459 LY-90459 4H-1-Benzopyran-4-one,7-hydroxy-3-(trifluoromethyl)- inflammation,LRCL-3794,monocyte migration,inhibit,COX,Cyclooxygenase,LRCL 3794,LRCL3794,Inhibitor,lipoxygenase,Benoxaprofen,antipyretic compound 2-[2-(4-Chlorophenyl)-5-benzoxazolyl]propanoic Acid 51234-28-7 Aromatics Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Isotope Labelled Compounds Phamaceuticals