3-CYANO-N-HYDROXY-BENZAMIDINE
3-Cyano-N-hydroxy-benzamidine
CAS: 453565-58-7
Molecular Formula: C8H7N3O
3-CYANO-N-HYDROXY-BENZAMIDINE - Names and Identifiers
| Name | 3-Cyano-N-hydroxy-benzamidine |
| Synonyms | 3-CYANO-N-HYDROXY-BENZAMIDINE 3-Cyano-N-hydroxy-benzamidine |
| CAS | 453565-58-7 |
3-CYANO-N-HYDROXY-BENZAMIDINE - Physico-chemical Properties
| Molecular Formula | C8H7N3O |
| Molar Mass | 161.16 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD09038677 |
3-CYANO-N-HYDROXY-BENZAMIDINE - Risk and Safety
| Hazard Class | IRRITANT |
3-CYANO-N-HYDROXY-BENZAMIDINE - Introduction
(3-cyanide-N-hydroxyl aniline) is an organic compound with a chemical formula of C8H7N3O. It is a colorless crystal with aniline-like amino groups and aniline formate hydroxyl groups.
This compound is commonly used in medicine and chemistry. It is a multifunctional organic reagent commonly used in the synthesis of other organic compounds. It has certain antibacterial and antiviral activities, so it is also used as an active fragment in drug development.
The method of preparing calcium can be by adding sodium hydroxide and dimethyl carbonate to aniline, and then reacting to generate N-hydroxyaniline dimethyl formate. This is then converted to the corresponding 3-cyano derivative. The specific synthesis scheme needs to be adjusted according to different reaction conditions and required purity.
Regarding safety information, it is a chemical reagent that needs to be handled carefully in the laboratory and avoid contact with skin and eyes. Appropriate personal protective equipment, such as lab gloves and safety glasses, should be worn. The safety data sheets should be read carefully before use and handled and stored in accordance with proper operating procedures.
This compound is commonly used in medicine and chemistry. It is a multifunctional organic reagent commonly used in the synthesis of other organic compounds. It has certain antibacterial and antiviral activities, so it is also used as an active fragment in drug development.
The method of preparing calcium can be by adding sodium hydroxide and dimethyl carbonate to aniline, and then reacting to generate N-hydroxyaniline dimethyl formate. This is then converted to the corresponding 3-cyano derivative. The specific synthesis scheme needs to be adjusted according to different reaction conditions and required purity.
Regarding safety information, it is a chemical reagent that needs to be handled carefully in the laboratory and avoid contact with skin and eyes. Appropriate personal protective equipment, such as lab gloves and safety glasses, should be worn. The safety data sheets should be read carefully before use and handled and stored in accordance with proper operating procedures.
Last Update：2024-04-09 20:02:46
