1039837-72-3
(3-Cyclohexyl-1,2,4-oxadiazol-5-yl)methylaminehydrochloride
CAS: 1039837-72-3
Molecular Formula: C9H15N3O
1039837-72-3 - Names and Identifiers
1039837-72-3 - Physico-chemical Properties
| Molecular Formula | C9H15N3O |
| Molar Mass | 181.23 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD12027095 |
1039837-72-3 - Risk and Safety
| Hazard Class | IRRITANT |
1039837-72-3 - Introduction
(3-Cyclohexyl-1,2,4-oxadiazol-5-yl)methylaminehydrochloride is an organic compound with the chemical formula C9H14N4O · HCl.
Nature:
(3-Cyclohexyl-1,2,4-oxadiazol-5-yl)methylaminehydrochloride is a white crystalline solid. It has low solubility and excellent stability, stable at room temperature. The compound is relatively stable in air, but may decompose under light.
Use:
(3-Cyclohexyl-1,2,4-oxadiazol-5-yl)methylaminehydrochloride is a potential pesticide intermediate. It can be used to synthesize other pesticides and has insecticidal and fungicidal activity.
Preparation Method:
(3-Cyclohexyl-1,2,4-oxadiazol-5-yl)methylaminehydrochloride can be synthesized by a series of chemical reactions. One possible synthesis is: First, 3-cyclohexyl-1, 2,4-oxadiazole-5-methanol is reacted with an appropriate base to form the corresponding amine derivative. Then, hydrochloric acid was added to form the hydrochloride.
Safety Information:
Nature:
(3-Cyclohexyl-1,2,4-oxadiazol-5-yl)methylaminehydrochloride is a white crystalline solid. It has low solubility and excellent stability, stable at room temperature. The compound is relatively stable in air, but may decompose under light.
Use:
(3-Cyclohexyl-1,2,4-oxadiazol-5-yl)methylaminehydrochloride is a potential pesticide intermediate. It can be used to synthesize other pesticides and has insecticidal and fungicidal activity.
Preparation Method:
(3-Cyclohexyl-1,2,4-oxadiazol-5-yl)methylaminehydrochloride can be synthesized by a series of chemical reactions. One possible synthesis is: First, 3-cyclohexyl-1, 2,4-oxadiazole-5-methanol is reacted with an appropriate base to form the corresponding amine derivative. Then, hydrochloric acid was added to form the hydrochloride.
Safety Information:
Last Update：2024-04-10 22:29:15
