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ChemicalBook--->CAS DataBase List--->60932-58-3

60932-58-3

60932-58-3 Structure

60932-58-3 Structure
IdentificationMore
[Name]

1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLIC ACID
[CAS]

60932-58-3
[Synonyms]

1H-1,2,3-BENZOTRIAZOLE-5-CARBOXYLIC ACID
1H-BENZOTRIAZOLE-5-CARBOXYLIC ACID
1-H-BENZOTRIAZOLECARBOXYLIC ACID
5-CARBOXYBENZOTRIAZOLE
5-CARBOXYL BENZOTRIAZOLE
BENZOTRIAZOLE-5-CARBOXYLIC ACID
BUTTPARK 98\57-27
COBRATEC(R) CBT
OTAVA-BB BB7117850639
ZERENEX E/6026513
[EINECS(EC#)]

262-527-4
[Molecular Formula]

C7H5N3O2
[MDL Number]

MFCD00012318
[Molecular Weight]

163.13
[MOL File]

60932-58-3.mol
Chemical PropertiesBack Directory
[InChI]

InChI=1S/C7H5N3O2/c11-7(12)4-1-2-5-6(3-4)9-10-8-5/h1-3H,(H,11,12)(H,8,9,10)
[InChIKey]

GUOVBFFLXKJFEE-UHFFFAOYSA-N
[SMILES]

N1C2=CC=C(C(O)=O)C=C2N=N1
[CAS DataBase Reference]

60932-58-3(CAS DataBase Reference)
[EPA Substance Registry System]

1H-Benzotriazolecarboxylic acid (60932-58-3)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Used as an intermediate for organic synthesis.
[Synthesis]

1H-Benzotriazole-5-carboxylic acid was formed of carboxytriazole (3.91 g, 24 mmol), 4-dimethylaminopyridine (0.32 g, 2.6 mmol), dimethylformamide (58 g) andatert-butyl methyl ether (46 g) solution of ZTETRAOL 2000s produced by the SOLVAY SOLEXIS company (Mn of 1730 for Rf(F)=-CF2O (CF2CF2O)m(CF2O)nCF2-) (13.26 g, 6.0 mmol) which had four terminal hydroxyl groups, as a perfluoropolyether were added sequentially to a three-necked flask which had been fitted with a nitrogen bubbling tube and a stirrer. 1-Ethy3- (3-dimethylaminopropyl)carboxylmide hydrochloride (4.60 g, 24 mmol) was added at room temperature and stirred for 24 hours at 50°C. Water (60 g) and methyl isobutyl ketone (60 g) were added to the reaction solution and the liquid was partitioned. The organic layer was washed two or three times with 1% hydrochloric acid aqueous solution (50 g) and saturated salt water (50 g) and then dried with anhydrous sodium sulphate and concentrated and 1H-Benzotriazole-5-carboxylic acid was obtained. Yield (10.1 g).
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