ethyl 3,5-dimethyl-1,2-oxazole-4-carboxylate

ethyl 3,5-dimethyl-1,2-oxazole-4-carboxylate - Names and Identifiers

Name	Ethyl 3,5-dimethylisoxazole-4-carboxylate
Synonyms	ethyl 3 RARECHEM AL BI 0516 5-diMethylisoxazole-4-carboxylate 3,5-Dimethyl-4-(ethoxycarbonyl)isoxazole ETHYL 3,5-DIMETHYLISOXAZOLE-4-CARBOXYLATE Ethyl 3,5-Dimethylsoxazole-4-carboxylate Ethyl 3,5-dimethylisoxazole-4-carboxylate ETHYL 3,5-DIMETHYL-4-ISOXAZOLECARBOXYLATE ethyl 3,5-dimethyl-1,2-oxazole-4-carboxylate 3,5-dimethyl-4-isoxazolecarboxylic acid ethyl ester
CAS	17147-42-1
InChI	InChI=1/C8H11NO3/c1-4-11-8(10)7-5(2)9-12-6(7)3/h4H2,1-3H3

ethyl 3,5-dimethyl-1,2-oxazole-4-carboxylate - Physico-chemical Properties

Molecular Formula	C8H11NO3
Molar Mass	169.18
Density	1?+-.0.06 g/cm3(Predicted)
Boling Point	88°C 2mm
Flash Point	87-89°C/2mm
Vapor Presure	0.0453mmHg at 25°C
pKa	-2.52±0.28(Predicted)
Storage Condition	2-8℃
Refractive Index	1.4600 to 1.4640
MDL	MFCD00052557

ethyl 3,5-dimethyl-1,2-oxazole-4-carboxylate - Risk and Safety

Safety Description	24/25 - Avoid contact with skin and eyes.
HS Code	29349990
Hazard Class	IRRITANT

ethyl 3,5-dimethyl-1,2-oxazole-4-carboxylate - Introduction

Ethyl 3 is an organic compound with the chemical formula C9H10N2O2. The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance: Ethyl 3, colorless to light yellow crystalline solid.
-Solubility: It is almost insoluble in water, but has good solubility in organic solvents (such as ethanol, methanol, xylene, etc.).
-Melting point: Its melting point is about 165-168 degrees Celsius.

Use:
- Ethyl 3, is a compound with antifungal activity, used in the pharmaceutical industry and agriculture. In pharmaceuticals, it is applied to the synthesis of antifungal drugs; In agriculture, it is used as an ingredient in pesticides or plant growth regulators.
-It can also be used as a raw material in the fields of fungicides, inhibitors and preservatives.

Method:
- Ethyl 3, there are many preparation methods. Common methods include chlorination reaction, oxidation reaction and esterification reaction of isoxazole.

Safety Information:
- Ethyl 3 is an organic compound. Pay attention to personal protective measures when exposed, such as wearing gloves and protective glasses.
-It has a certain degree of irritation and may cause irritation to the skin and eyes, so direct contact with the skin and eyes should be avoided during use.
-During storage and handling, avoid contact with strong oxidants and high temperatures to avoid danger.
-If necessary, operate in a well-ventilated environment and avoid inhaling dust or vapor.

Last Update：2024-04-09 20:49:11