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| 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 |
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