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5-BroMo-1H-indazole-3-car...

5-Bromo-1H-Indazole-3-Carboxylic Acid

CAS: 1077-94-7

Molecular Formula: C8H5BrN2O2

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5-BroMo-1H-indazole-3-car... - Names and Identifiers

Name 5-Bromo-1H-Indazole-3-Carboxylic Acid
Synonyms 5-BroMo-1H-indazole-3-car...
5-Bromo-3-carboxy-1H-indazole
5-BROMOINDAZOLE-3-CARBOXYLIC ACID
5-BROMO-3-INDAZOLECARBOXYLIC ACID
5-Bromoindazole-3-Carboxylic Acid
5-Bromo-3-Indazolecarboxylic Acid
5-broMo-1H-indazol-3-carboxylic acid
5-Bromo-1H-Indazole-3-Carboxylic Acid
5-BROMO-1H-INDAZOLE-3-CARBOXYLIC ACID
5-bromobenzopyrazole-3-carboxylic acid
1H-INDAZOLE-3-CARBOXYLIC ACID, 5-BROMO-
1H-Indazole-3-Carboxylic Acid, 5-Bromo-
CAS 1077-94-7
InChI InChI=1/C8H5BrN2O2/c9-4-1-2-6-5(3-4)7(8(12)13)11-10-6/h1-3H,(H,10,11)(H,12,13)

5-BroMo-1H-indazole-3-car... - Physico-chemical Properties

Molecular FormulaC8H5BrN2O2
Molar Mass241.04
Density1.946±0.06 g/cm3(Predicted)
Melting Point289-292°C
Boling Point493.4±25.0 °C(Predicted)
Flash Point252.176°C
Vapor Presure0mmHg at 25°C
AppearanceCrystalline powder
pKa2.81±0.30(Predicted)
Storage Condition2-8°C
Refractive Index1.766
MDLMFCD05663979

5-BroMo-1H-indazole-3-car... - Risk and Safety

Risk Codes22 - Harmful if swallowed
Safety DescriptionS22 - Do not breathe dust.
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.
Hazard NoteIrritant

5-BroMo-1H-indazole-3-car... - Reference Information

uses various derivatives of indazole -3-carboxylic acid also have biological activities such as anti-spermatogenesis, anti-arthritis and antiemetic activities, among which granisetron hydrochloride is a highly selective 5-HT, receptor antagonist, which has been widely used to prevent and treat nausea and vomiting caused by chemotherapy in tumor patients. In recent years, with the rapid development of the pharmaceutical industry, 5-bromoindazole -3-carboxylic acid as an important chemical product has received more and more attention.
Preparation Method for synthesizing 5-bromoindazole-3-formic acid with 5-bromoisatin as the starting material: Mix the alkaline solution of 5-bromoisatin with sodium nitrite solution, add it to dilute sulfuric acid solution under cooling for diazotization, the resulting diazonium salt solution is saturated with sulfur dioxide and reduced with stannous chloride to obtain 5-bromoindazole-3-formic acid. It is difficult to remove a large amount of tin-containing impurities in the obtained crude product, which can be refined by repeated recrystallization with glacial acetic acid. the synthesis reaction formula is as follows: fig. 1 5-bromoindazole -3-formic acid synthesis reaction formula
Last Update:2024-04-09 20:49:11
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