ChemicalBook >> CAS DataBase List >>FENTIAZAC

FENTIAZAC

CAS No.
18046-21-4
Chemical Name:
FENTIAZAC
Synonyms
ch800;br700;flogene;donorest;norvedan;FENTIAZAC;4-(4-chlorophenyl)-2-phenyl-5-thiazoleaceticaci;4-(p-chlorophenyl)-2-phenyl-5-thiazoleaceticaci;4-(p-chlorophenyl)-2-phenylthiazole-5-aceticacid;4-(p-chlorophenyl)-2-phenyl-5-thiazoleaceticacid
CBNumber:
CB8736909
Molecular Formula:
C17H12ClNO2S
Molecular Weight:
329.8
MDL Number:
MFCD00866039
MOL File:
18046-21-4.mol
Last updated:2023-05-04 17:34:35

FENTIAZAC Properties

Melting point 162°C
Boiling point 556.2±60.0 °C(Predicted)
Density 1.1592 (rough estimate)
refractive index 1.6100 (estimate)
pka 3.89±0.10(Predicted)
Water Solubility 31.66mg/L(25 ºC)
FDA UNII 0YHF6E6NLS
ATC code M01AB10,M02AA14

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
Risk Statements  36/37/38
Safety Statements  26-36/37/39
Toxicity LD50 in rats, mice (mg/kg): 661, 692 orally (Marmo)

FENTIAZAC price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation API0002696 FENTIAZAC 95.00% 18046-21-4 10MG $255.15 2021-12-16 Buy
Crysdot CD11215310 2-(4-(4-Chlorophenyl)-2-phenylthiazol-5-yl)aceticacid 95% 18046-21-4 1g $317 2021-12-16 Buy
AHH MT-51775 Fentiazac 98% 18046-21-4 0.1g $350 2021-12-16 Buy
Crysdot CD11215310 2-(4-(4-Chlorophenyl)-2-phenylthiazol-5-yl)aceticacid 95% 18046-21-4 5g $624 2021-12-16 Buy
Crysdot CD11215310 2-(4-(4-Chlorophenyl)-2-phenylthiazol-5-yl)aceticacid 95% 18046-21-4 10g $942 2021-12-16 Buy
Product number Packaging Price Buy
API0002696 10MG $255.15 Buy
CD11215310 1g $317 Buy
MT-51775 0.1g $350 Buy
CD11215310 5g $624 Buy
CD11215310 10g $942 Buy

FENTIAZAC Chemical Properties,Uses,Production

Originator

Norvedan,LPB,Italy,1975

Uses

Anti-inflammatory.

Definition

ChEBI: 2-[4-(4-chlorophenyl)-2-phenyl-5-thiazolyl]acetic acid is a member of thiazoles.

Manufacturing Process

13.6 g methyl 3-(p-chlorobenzoyl)-3-bromopropionate in 30 ml methanol are added to a solution of 5.6 g potassium thioacetate in 30 ml methanol. Immediate precipitation of KBr is observed. The suspension is refluxed for 10 minutes.
It is cooled to ambient temperature, filtered, and the methanol is evaporated to dryness. 13.2 g methyl 3-(p-chlorobenzoyl)-3-thioacetylpropionate in the form of a chromatographically pure orange-colored oil are obtained.
A suspension of 13.2 g methyl 3-(p-chlorobenzoyl)-3-thioacetylpropionate is agitated in 500 ml of a 2 N aqueous solution of KOH for 6 hours at ambient temperature in an atmosphere of nitrogen, followed by extraction with ethyl ether. The aqueous phase, adjusted to a pH equal to 2 with 2N HCl, is extracted with ethyl ether which was washed with water, dried over Na2SO4, and finally evaporated to dryness
9.8 g of crude 3-(p-chlorobenzoyl)-3-mercaptopropionic acid are obtained. By recrystallizing from isopropyl ether there are obtained 8.6 g of pure product, MP 96°C to 97°C (yield: 79%).
1.7 ml benzonitrile and 5.05 ml diethylamine are added to a solution of 4 g 3- (p-chlorobenzoyl)-3-thiol-propionic acid in 50 ml ethanol. The solution is agitated at ambient temperature for 60 minutes in an atmosphere of nitrogen. It is then evaporated to a syrupy consistency and 60 ml 50% aqueous acetic acid are added, whereupon the mixture is refluxed for 60 minutes. It is evaporated to a small volume, adjusted to a pH equal to 8 with a saturated solution of sodium bicarbonate and then extracted with ethyl ether. The aqueous phase is acidified with 2N HCl (Congo red), and then again extracted with ethyl ether. It is dried over Na2SO4 and evaporated to dryness. The evaporation residue is recrystallized from benzene and 4 g 4-(p-chlorophenyl)- 2-phenyl-thiazol-5-yl-acetic acid are obtained (MP = 152°C to 154°C, yield - 74.3%).

Therapeutic Function

Analgesic, Antipyretic, Antiinflammatory

General Description

Fentiazac is reported to have anti-inflammatory, analgesic, and antipyretic activity. It has been given once or twice a day at levels between 100 and 200 mg/dose in the treatment of postoperative pain, including that following orthopedic surgery. The most common adverse effect is gastrointestinal intolerance, including epigastric pain, nausea, and vomiting. Effects on the CNS, such as headache and dizziness, also have been reported.

Trade name

Atilan (Zambon, Brazil), Donorest (Fontoura-Wyeth, Brazil), Flogene (Polifarma, Italy), Norvedan (Boehringer Mannheim, Austria; LPB, Italy).

Synthesis

Synthesis: refluxing a mixture of 3-bromo- 3-(4-chlorobenzoyl)propionic acid and thiobenzamide in ethanol gives ethyl 2-phenyl-4-(4- chlorophenyl)thiazole-5-acetate, which is then saponified to yield fentiazac.
synthesis of FENTIAZAC

FENTIAZAC Preparation Products And Raw materials

FENTIAZAC Suppliers

Global( 16)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Finetech Industry Limited
+86-27-87465837 +8618971612321 info@finetechnology-ind.com China 9633 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923 1026@dideu.com China 9116 58
Finetech Industry Limited 027-87465837 19945049750 sales@finetechnology-ind.com China 9636 58
Shanghai Haohong Pharmaceutical Co., Ltd. 400-400-8210725 4008210725 malulu@leyan.com China 55023 58
Shaanxi Xihua Chemical Industry Co., Ltd 17691182729 15529505138 1021@dideu.com China 10011 58
FENTIAZAC 4-(4-chlorophenyl)-2-phenyl-5-thiazoleaceticacid 4-(p-chlorophenyl)-2-phenyl-5-thiazoleaceticaci 4-(p-chlorophenyl)-2-phenyl-5-thiazoleaceticacid 4-(p-chlorophenyl)-2-phenylthiazole-5-aceticacid 4-(4-Chlorlphenyl)-2-phenyl-5-thiazoleacetic acid br700 ch800 donorest 4-(4-chlorophenyl)-2-phenyl-5-thiazoleaceticaci flogene norvedan [4-(4-Chloro-phenyl)-2-phenyl-thiazol-5-yl]-acetic acid 5-Thiazoleacetic acid, 4-(4-chlorophenyl)-2-phenyl- 18046-21-4 8046-21-4