ChemicalBook--->CAS DataBase List--->22232-54-8

22232-54-8

22232-54-8 Structure

22232-54-8 Structure
IdentificationMore
[Name]

Carbimazole
[CAS]

22232-54-8
[Synonyms]

1-ETHOXYCARBONYL-3-METHYL-2-THIOXO-4-IMIDAZOLINE
CARBIMAZOLE
ETHYL 3-METHYL-2-THIOMIDAZOLINE-1-CARBOXYLATE
ETHYL 3-METHYL-2-THIONOIMIDAZOLINE-1-CARBOXYLATE
LABOTEST-BB LT00455569
1H-Imidazole-1-carboxylic acid, 2,3-dihydro-3-methyl-2-thioxo-, ethyl ester
1h-imidazole-1-carboxylicacid,2,3-dihydro-3-methyl-2-thioxo,ethylester
2,3-Dihydro-3-methyl-2-thioxo-1H-imidazole-1-carboxylicacidethylester
2-Carbethoxythio-1-methylimidazole
3-Methyl-2-thioxo-4-imidazoline-1-carboxylic acid ethyl ester
3-methyl-2-thioxo-4-imidazoline-1-carboxylicacidethylester
3-methyl-2-thioxo-4-imidazoline-1-carboxylicaciethylester
4-Imidazoline-1-carboxylic acid, 3-methyl-2-thioxo-, ethyl ester
Athyromazole
Basolest
Carbethoxymethimazole
Carbimazol
Carbinazole
CG1
Ethyl 3-methyl-2-thioimidazoline-1-carboxylate
[EINECS(EC#)]

244-854-4
[Molecular Formula]

C7H10N2O2S
[MDL Number]

MFCD00027421
[Molecular Weight]

186.23
[MOL File]

22232-54-8.mol
Chemical PropertiesBack Directory
[Melting point ]

124°C
[Boiling point ]

240.4±23.0 °C(Predicted)
[density ]

1.2900 (rough estimate)
[refractive index ]

1.5400 (estimate)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO: soluble5mg/mL, clear (warmed)
[form ]

powder
[pka]

-1.70±0.20(Predicted)
[color ]

white to beige
[Water Solubility ]

Soluble in water, ethanol, chloroform and acetone. Sightly soluble in water.
[Sensitive ]

Light Sensitive
[Merck ]

14,1798
[BRN ]

144339
[InChIKey]

CFOYWRHIYXMDOT-UHFFFAOYSA-N
[CAS DataBase Reference]

22232-54-8(CAS DataBase Reference)
[NIST Chemistry Reference]

Carbimazole(22232-54-8)
Safety DataBack Directory
[Risk Statements ]

R22:Harmful if swallowed.
R36:Irritating to the eyes.
R43:May cause sensitization by skin contact.
[Safety Statements ]

S22:Do not breathe dust .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RIDADR ]

3335
[WGK Germany ]

3
[RTECS ]

NJ2441000
[HS Code ]

2933.29.9000
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Methylamine-->Ethyl chloroformate-->Potassium thiocyanate-->Chloroacetaldehyde diethyl acetal-->2-MERCAPTOIMIDAZOLE-->Pyridine-->(2,2-diethoxyethyl)methylamine
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Originator]

Carbimazol,Cid Co.
[Uses]

Carbimazole, a prodrug of Methimazole (M260300), is used in the treatment of hyperthyroidism.
[Uses]

Thionamide antithyroid drug.
[Definition]

ChEBI: A member of the class of imidazoles that is methimazole in which the nitrogen bearing a hydrogen is converted into its ethoxycarbonyl derivative. A prodrug for methimazol, carbimazole is used for the treatment of hyperthyroidism.
[Manufacturing Process]

0.1 mol of 1-methyl-2-mercaptoglyoxaline is dissolved in the minimum quantity of pyridine at 0°C 0.1 mol of ethyl chloroformate is added drop wise with stirring. More pyridine is added, if necessary, to keep the mixture semi-fluid. The sludge is then placed in an ice bath for 30 minutes. The crystals are filtered off and washed firstly with a little ethanol and secondly with ethanol and water. The non-basic desired ethyl 3-methyl-2-thioimidazoline-1- carboxylate is the colourless needles having a melting point of 122°-123°C.
[Therapeutic Function]

Thyroid inhibitor
[Clinical Use]

Treatment of hyperthyroidism
[Synthesis]

Carbimazole, the ethyl ester of 3-methyl-2-thioimidazolin-1-carboxylic acid (25.2.7), is synthesized by a simultaneous reaction of ethylenacetal of bromoacetaldehyde with methylamine and potassium isocyanate, forming 3-methyl-2-imidazolthione (25.2.6), which is further acylated at the nitrogen atom by ethyl chloroformiate, giving the desired product (25.2.7).

Synthesis_22232-54-8

[Veterinary Drugs and Treatments]

Carbimazole (a pro-drug of methimazole) or methimazole are considered by most clinicians to be the agents of choice when using drugs to treat feline hyperthyroidism. Propylthiouracil has significantly higher incidences of adverse reactions when compared to methimazole.
Methimazole and therefore, carbimazole, may be useful for the prophylactic prevention of cisplatin-induced nephrotoxicity in dogs.
[Drug interactions]

Potentially hazardous interactions with other drugs None known
[Metabolism]

Carbimazole is rapidly metabolised to thiamazole, which is concentrated in the thyroid gland. Over 90% of orally administered carbimazole is excreted in the urine as thiamazole or its metabolites. The remainder appears in faeces. There is 10% enterohepatic circulation. Thiamazole is metabolised, probably by the liver, and excreted in the urine. Less than 12% of a dose of thiamazole may be excreted as unchanged drug
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

Carbimazole(22232-54-8)MS
Carbimazole(22232-54-8)1HNMR
Carbimazole(22232-54-8)13CNMR
Carbimazole(22232-54-8)IR1
Carbimazole(22232-54-8)IR2
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

Ethyl 3-methyl-2-thionoimidazoline-1-carboxylate, 97%(22232-54-8)
[TCI AMERICA]

Carbimazole,>99.0%(GC)(22232-54-8)
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