1186647-69-7
4-Chloro-3-iodo-1H-pyrazolo[4,3-c]pyridine
CAS: 1186647-69-7
Molecular Formula: C6H3ClIN3
1186647-69-7 - Names and Identifiers
1186647-69-7 - Physico-chemical Properties
| Molecular Formula | C6H3ClIN3 |
| Molar Mass | 279.47 |
| Density | 2.284 |
| Boling Point | 435.2±40.0 °C(Predicted) |
| pKa | 8.51±0.40(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
1186647-69-7 - Risk and Safety
| Risk Codes | 36 - Irritating to the eyes |
| Safety Description | 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
| UN IDs | UN 2811 6.1 / PGIII |
1186647-69-7 - Introduction
4-Chloro-3-iodo-1H-pyrazolo [4,3-C] pyridine is an organic compound with the chemical formula C9H4ClI and a molecular weight of 311.49g/mol. It has the structure of a pyrazolo [4,3-C] pyridine in which one carbon atom is attached to the pyrazole and pyridine rings.
Properties of the compound include:
-Appearance: Colorless to yellow crystal
-melting point: about 190-200 ℃
-Boiling point: about 280 ℃
-Solubility: Insoluble in water, but soluble in some organic solvents such as ethanol and dichloromethane.
The uses of 4-chloro-3-iodo-1H-pyrazolo [4,3-C] pyridine mainly include as intermediates and reagents in organic synthesis. It can be used in the synthesis of other nitrogen-containing heterocyclic compounds and organometallic complexes, such as the preparation of pyrazine drugs and coordination compounds.
The method of preparing 4-chloro-3-iodo-1H-pyrazolo [4,3-C] pyridine is usually accomplished by an organic synthesis reaction. A common method is the reaction of 3-bromo-4-chloro-5-iodopyridine with potassium permanganate in methylene chloride through a series of steps to form the desired product.
When using 4-chloro-3-iodo-1H-pyrazolo [4,3-C] pyridine, you need to pay attention to the following safety information:
-This compound may cause irritation and damage to the human body. Contact with skin, eyes, mouth and nose should be avoided.
-need to operate in a well-ventilated environment, avoid inhalation of its vapor or dust.
-Use with appropriate personal protective equipment, such as lab gloves, goggles and protective masks.
-Waste should be disposed of properly and in compliance with relevant laws and regulations.
Since 4-chloro-3-iodo-1H-pyrazolo [4,3-C] pyridine is an organic compound, it is recommended to use and handle this compound under suitable laboratory conditions and follow Relevant safety procedures.
Properties of the compound include:
-Appearance: Colorless to yellow crystal
-melting point: about 190-200 ℃
-Boiling point: about 280 ℃
-Solubility: Insoluble in water, but soluble in some organic solvents such as ethanol and dichloromethane.
The uses of 4-chloro-3-iodo-1H-pyrazolo [4,3-C] pyridine mainly include as intermediates and reagents in organic synthesis. It can be used in the synthesis of other nitrogen-containing heterocyclic compounds and organometallic complexes, such as the preparation of pyrazine drugs and coordination compounds.
The method of preparing 4-chloro-3-iodo-1H-pyrazolo [4,3-C] pyridine is usually accomplished by an organic synthesis reaction. A common method is the reaction of 3-bromo-4-chloro-5-iodopyridine with potassium permanganate in methylene chloride through a series of steps to form the desired product.
When using 4-chloro-3-iodo-1H-pyrazolo [4,3-C] pyridine, you need to pay attention to the following safety information:
-This compound may cause irritation and damage to the human body. Contact with skin, eyes, mouth and nose should be avoided.
-need to operate in a well-ventilated environment, avoid inhalation of its vapor or dust.
-Use with appropriate personal protective equipment, such as lab gloves, goggles and protective masks.
-Waste should be disposed of properly and in compliance with relevant laws and regulations.
Since 4-chloro-3-iodo-1H-pyrazolo [4,3-C] pyridine is an organic compound, it is recommended to use and handle this compound under suitable laboratory conditions and follow Relevant safety procedures.
Last Update：2024-04-09 19:05:45
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