878011-44-0 - Names and Identifiers
Name | 3H-IMidazo[4,5-b]pyridine-3-carboxylic acid, 7-chloro-5-nitro-, 1,1-diMethylethyl ester
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Synonyms | 3-Boc-7-chloro-5-nitro-3H-imidazo[4,5-b]pyridine tert-butyl 7-chloro-5-nitro-imidazo[4,5-b]pyridine-3-carboxylate tert-Butyl 7-chloro-5-nitro-3H-imidazo-[4,5-b]pyridine-3-carboxylate 3H-IMidazo[4,5-b]pyridine-3-carboxylic acid, 7-chloro-5-nitro-, 1,1-diMethylethyl ester
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CAS | 878011-44-0
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878011-44-0 - Physico-chemical Properties
Molecular Formula | C11H11ClN4O4
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Molar Mass | 298.68 |
Density | 1.53±0.1 g/cm3(Predicted) |
Boling Point | 431.6±55.0 °C(Predicted) |
pKa | -1.20±0.30(Predicted) |
Storage Condition | 2-8℃ |
878011-44-0 - Introduction
3H-IMidazo[4,5-b]pyridine-3-carboxylic acid, 7-choro-5-nitro-, 1,1-diMethylethyl ester is an organic compound, its molecular formula is C13H15ClN4O4 and its molecular weight is 328.73g/mol.
Nature:
3H-IMidazo[4,5-b]pyridine-3-carboxylic acid, 7-chloro-5-nitro-, 1,1-diMethylethyl ester is a yellow to orange crystalline powder with flammability. It can form a clear solution when dissolved in organic solvents such as dimethyl sulfoxide and methanol.
Use:
3H-IMidazo[4,5-b]pyridine-3-carboxylic acid, 7-chroo-5-nitro-, 1,1-diMethylethyl ester is an organic synthesis intermediate widely used in the field of drug research and manufacturing. It can be used as a raw material for antibacterial drugs, antitumor drugs, antiviral drugs, etc. In addition, it can also be used as a catalyst and reagent in organic synthesis reactions.
Preparation Method:
3H-IMidazo[4,5-b]pyridine-3-carboxylic acid, 7-choro-5-nitro-, 1,1-diMethylethyl ester is prepared by a variety of methods, usually through a series of organic synthesis steps. A common preparation method is to react an appropriate amount of 7-chloro-5-nitroimidazo [4,5-c] pyridine-3-carboxylic acid with tert-butyl alcohol ester to obtain the target product.
Safety Information:
3H-IMidazo[4,5-b]pyridine-3-carboxylic acid, 7-choro-5-nitro-, 1,1-diMethylethyl ester is an organic compound with high toxicity and sensitization. Wear protective equipment during operation to avoid skin contact and inhalation. Avoid contact with oxidants and strong acids to avoid dangerous chemical reactions. Appropriate safety procedures shall be observed during storage and handling. If not used correctly, it may cause harm to the human body, which can lead to irritation, allergy or poisoning.
Last Update:2024-04-09 20:52:54