|
| | Ethyl 2-butynoate Basic information |
| | Ethyl 2-butynoate Chemical Properties |
| Boiling point | 160-161 °C/730 mmHg (lit.) | | density | 0.962 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.436(lit.) | | Fp | 145 °F | | storage temp. | Inert atmosphere,2-8°C | | solubility | Chloroform, Ethyl Acetate | | form | Powder | | Specific Gravity | 0.962 | | color | Grey to red to brown | | Water Solubility | Miscible with water, chloroform and ethyl acetate. | | Sensitive | Air Sensitive | | BRN | 1744948 | | InChIKey | FCJJZKCJURDYNF-UHFFFAOYSA-N | | CAS DataBase Reference | 4341-76-8(CAS DataBase Reference) | | NIST Chemistry Reference | Ethyl 2-butynoate(4341-76-8) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | RIDADR | 1993 | | WGK Germany | 3 | | F | 10-23 | | Hazard Note | Irritant | | HazardClass | 3.2 | | PackingGroup | III | | HS Code | 29161900 |
| | Ethyl 2-butynoate Usage And Synthesis |
| Uses | Ethyl 2-butynoate is used as a precursor for the synthesis of 3-ethyl, 1-methyl 1-(2-nitrophenyl)-cyclopent-3-ene-1,3-dicarboxylate, alkenylsilanols and tricyclic aziridine derivatives. It acts as a methanogenesis inhibitor. As an electron deficient alkyne derivative, it plays a vital role in the preparation of 1,3-dienes catalyzed by rhodium(I)/H8-BINAP complex. | | Uses | Ethyl 2-butynoate was used in the study of its effect on in vitro degradation and microbial biomass production. It may be used in the synthesis of the following:
- 3-ethyl, 1-methyl 1-(2-nitrophenyl)-cyclopent-3-ene-1,3-dicarboxylate
- tricyclic aziridine derivatives
- alkenylsilanols
| | Synthesis Reference(s) | Organic Syntheses, Coll. Vol. 7, p. 226, 1990 The Journal of Organic Chemistry, 38, p. 3588, 1973 DOI: 10.1021/jo00960a032 | | General Description | Ethyl 2-butynoate, a 2-alkynoate is a methanogenesis inhibitor. It is an electron deficient internal alkyne that has been reported to undergo codimerization with alkenes to form 1,3-dienes catalyzed by rhodium(I)/H8-BINAP complex. The annulation of thioamides with ethyl 2-butynoate catalyzed by tri-n-butylphosphine to form thiazolines has been investigated. |
| | Ethyl 2-butynoate Preparation Products And Raw materials |
|