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Cinchophen

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Name

Cinchophen

EINECS N/A
CAS No. 132-60-5 Density 1.28g/cm3
PSA 50.19000 LogP 3.60000
Solubility Insoluble in water Melting Point 214-215 °C(lit.)

Formula C16H11 N O2 Boiling Point 456.9°Cat760mmHg
Molecular Weight 249.269 Flash Point 230.1°C
Transport Information N/A Appearance N/A
Safety A human poison by ingestion. An experimental poison by intraperitoneal and subcutaneous routes. Moderately toxic by an unspecified route. When heated to decomposition it emits toxic fumes of NOx. Risk Codes 22
Molecular Structure Molecular Structure of 132-60-5 (CINCHOPHEN) Hazard Symbols
Synonyms

Cinchoninicacid, 2-phenyl- (8CI); 2-Phenyl-4-quinolinecarboxylic acid; 2-Phenylcinchonicacid; 2-Phenylcinchoninic acid; 4-Carboxy-2-phenylquinoline; Aciphenochinoline;Aciphenochinolinium; Agotan; Alutyl; Alutyo; Aminophan; Artam; Artexin; Atigoa;Atocin; Atofan; Atophan; Cinchophen; Cinchophene; Cinchophenic acid; Cinconal;Cincophen; Cincosal; Ikterosan; Mylofanol; NSC 2617; NSC 70178; Phenophan;Phenoquin; Polyphlogin; Quinofen; Quinophan; Quinophen; Rhematan; Rheumatan;Rheumin; Rheumine; Tervalon; Tophol; Tophosan; Traubofan; Vantyl; Viophan

Article Data 87

Cinchophen Synthetic route

5467-57-2

2-chloroquinoline-4-carboxylic acid

98-80-6

phenylboronic acid

132-60-5

cinchophen

Conditions
ConditionsYield
With potassium carbonate In ethanol; water at 50℃; for 4h; Suzuki-Miyaura coupling reaction; Inert atmosphere;96%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In 1,4-dioxane; water at 140℃; for 0.5h; Suzuki-Miyaura Coupling; Inert atmosphere; Microwave irradiation;
91-56-5

indole-2,3-dione

98-86-2

acetophenone

132-60-5

cinchophen

Conditions
ConditionsYield
With potassium hydroxide In ethanol; water for 0.208333h; microwave irradiation;95%
Stage #1: indole-2,3-dione With cetyltrimethylammonium hydroxide In water at 20℃; for 0.166667h; Pfitzinger Quinoline Synthesis; Sonication; Green chemistry;
Stage #2: acetophenone In water at 35℃; for 2.5h; Solvent; Reagent/catalyst; Temperature; Pfitzinger Quinoline Synthesis; Sonication; Green chemistry;
95%
With potassium hydroxide In ethanol at 50 - 60℃; for 14h;90%
5467-57-2

2-chloroquinoline-4-carboxylic acid

960-16-7

tributylphenylstannane

132-60-5

cinchophen

Conditions
ConditionsYield
With cesium fluoride In ethanol; water at 50℃; for 5h; Stille coupling; Inert atmosphere;92%
88730-73-8

3-Hydroxy-3-(2-oxo-2-phenyl-ethyl)-1,3-dihydro-indol-2-one

132-60-5

cinchophen

Conditions
ConditionsYield
With sulfuric acid In acetic acid for 5h; Heating;90%
With potassium hydroxide; ethanol
100-52-7

benzaldehyde

127-17-3

2-oxo-propionic acid

62-53-3

aniline

132-60-5

cinchophen

Conditions
ConditionsYield
With toluene-4-sulfonic acid In ethanol for 0.05h; Reagent/catalyst; Solvent; Microwave irradiation; Green chemistry;80%
With ytterbium perfluorooctanoate In water for 3h; Doebner reaction; Reflux;72%
In ethanol for 3h; Reflux;51%
100-52-7

benzaldehyde

127-17-3

2-oxo-propionic acid

132-60-5

cinchophen

Conditions
ConditionsYield
Stage #1: benzaldehyde; 2-oxo-propionic acid With acetic acid for 1h; Reflux;
Stage #2: With aniline for 8h; Reflux;
62.2%
117839-38-0

2-phenyl-4-quinolinecarboxaldehyde

A

29268-33-5

4-hydroxymethyl-2-phenylquinoline

B

132-60-5

cinchophen

Conditions
ConditionsYield
With potassium hydroxide; ethanol; water
With potassium hydroxide; ethanol; water
31541-36-3, 34880-79-0, 56680-29-6

3-(2-oxo-2-phenyl-ethylidene)-1,3-dihydro-indol-2-one

132-60-5

cinchophen

Conditions
ConditionsYield
With hydrogenchloride; ethanol; water
With ethanol; water; potassium carbonate
960-53-2

1,5-diphenyltetrahydro-2,3-pyrroledione

100-52-7

benzaldehyde

132-60-5

cinchophen

Conditions
ConditionsYield
With ethanol; acetic acid; aniline
70097-13-1

2-(4-nitrophenyl)quinoline-4-carboxylic acid

132-60-5

cinchophen

Conditions
ConditionsYield
beim Nitrieren;

Cinchophen Chemical Properties

Empirical Formula: C16H11NO2
Molecular Weight: 249.264 g/mol
EINECS: 205-067-1
Melting point: 214-215 °C(lit.)
Sensitive: Light sensitive
Index of Refraction: 1.682
Density: 1.28 g/cm3
Flash Point: 230.1 °C
Enthalpy of Vaporization: 75.55 kJ/mol
Boiling Point: 456.9 °C at 760 mmHg
Vapour Pressure: 3.84E-09 mmHg at 25 °C 
Structure of Cinchophen (CAS NO.132-60-5):
                    
IUPAC Name: 2-Phenylquinoline-4-carboxylic acid
Product Categories: API intermediates;Quinolinecarboxylic Acids

Cinchophen Uses

 Cinchophen (CAS NO.132-60-5) has been used as antipyretic analgesic for acute and chronic arthritis, rheumatic pain, neuralgia, lumbago, gout, headache and so on.

Cinchophen Production

First, having the preparation of isatin to be its sodium salt, and generated by the open-loop, and then with the cyclization of acetophenone to get Sim sodium , or with acetic acid or hydrochloric acid can be derived Xin-fen .

Cinchophen Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
dog LD50 oral 1250mg/kg (1250mg/kg)   Gekkan Yakuji. Pharmaceuticals Monthly. Vol. 9, Pg. 759, 1967.
human LDLo oral 214mg/kg (214mg/kg)   "Toxicology of Drugs and Chemicals," Deichmann, W.B., New York, Academic Press, Inc., 1969Vol. -, Pg. 177, 1969.
man LDLo unreported 74mg/kg (74mg/kg)   "Poisoning; Toxicology, Symptoms, Treatments," 2nd ed., Arena, J.M., Springfield, IL, C.C. Thomas, 1970Vol. 2, Pg. 73, 1970.
mouse LD50 intraperitoneal 200mg/kg (200mg/kg)   National Technical Information Service. Vol. AD691-490,
mouse LD50 subcutaneous 350mg/kg (350mg/kg)   Archives Internationales de Pharmacodynamie et de Therapie. Vol. 116, Pg. 154, 1958.
mouse LDLo oral 1500mg/kg (1500mg/kg)   "Narkoseversuche mit Hoheren Alkoholen und Stickstoffderivaten, Dissertation," Leube, F., Pharmakologischen Institut der Universitat Tubingen, Fed. Rep. Ger., 1931Vol. -, Pg. -, 1931.
rabbit LDLo unreported 500mg/kg (500mg/kg) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD Journal of Pharmacology and Experimental Therapeutics. Vol. 74, Pg. 365, 1942.
rat LD50 intravenous 600mg/kg (600mg/kg)   Gekkan Yakuji. Pharmaceuticals Monthly. Vol. 9, Pg. 759, 1967.
rat LDLo oral 500mg/kg (500mg/kg)   Journal of Pharmacology and Experimental Therapeutics. Vol. 90, Pg. 260, 1947.

 Cinchophen (CAS NO.132-60-5) hasn't been listed as a carcinogen by NTP, IARC, ACGIH, or CA Prop 65. And the toxicological properties have not been fully investigated. You can see actual entry in RTECS for complete information.

Cinchophen Safety Profile

A human poison by ingestion. An experimental poison by intraperitoneal and subcutaneous routes. Moderately toxic by an unspecified route. When heated to decomposition it emits toxic fumes of NOx.
Hazard Codes of Cinchophen (CAS NO.132-60-5): HarmfulXn
Risk Statements: 22 
R22:Harmful if swallowed.
Safety Statements: 36/37/39-26 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection.

Cinchophen Specification

 Cinchophen ,its cas register number is 132-60-5. It also can be called Cinchoninic acid, 2-phenyl- ; and 4-Quinolinecarboxylic acid, 2-phenyl- . 1g of the product can be dissolved in about 400ml chloroform, 100ml ether, 120ml of ethanol, almost insoluble in water. It is hazardous,so the first aid measures and others should be known. Such as: When on the skin: first,should flush skin with plenty of water immediately for at least 15 minutes while removing contaminated clothing. Secondly,Get medical aid. Or in the eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Then get medical aid soon. While ,it's Inhaled: Remove from exposure and move to fresh air immediately.Give artificial respiration while not breathing. When breathing is difficult, give oxygen. And as soon as to get medical aid. Then you have the ingesting of the product : Wash mouth out with water,and get medical aid immediately.Notes to physician: Treat supportively and symptomatically.
In addition, Cinchophen (CAS NO.132-60-5) may discolor on exposure to light. It is not compatible with strong oxidizing agents, strong bases, and you must not take it with incompatible materials. And also prevent it to broken down into hazardous decomposition products: nitrogen oxides, carbon monoxide, carbon dioxide.

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