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431:. It is a colorless liquid that is miscible with organic solvents. The compound is a reagent and building block for the synthesis of other organic compounds, reactions that exploit the electrophilicity of the alkyne group.
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372:103–105 °C (217–221 °F; 376–378 K)
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454:Encyclopedia of Reagents for Organic Synthesis
449:Encyclopedia of Reagents for Organic Synthesis
447:Hirst, Gavin C. (2001). "Methyl Propiolate".
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272:Key: IMAKHNTVDGLIRY-UHFFFAOYSA-N
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269:InChI=1S/C4H4O2/c1-3-4(5)6-2/h1H,2H3
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382:(at 25 °C , 100 kPa).
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52:methyl acetylenecarboxylate
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427:, the simplest acetylenic
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463:10.1002/047084289X.rm237
362:0.945 g mL
41:Methyl prop-2-ynoate
37:Preferred IUPAC name
404:with the formula HC
344: g·mol
111:Beilstein Reference
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502:Carboxylate esters
492:Alkyne derivatives
386:Infobox references
17:Methyl propiolate
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398:Methyl propiolate
394:Chemical compound
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352:colorless liquid
225:CompTox Dashboard
99:Interactive image
50:methyl propynoate
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402:organic compound
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58:Identifiers
48:Other names
349:Appearance
302:Properties
149:100.011.894
486:Categories
472:0471936235
435:References
337:Molar mass
293:COC(=O)C#C
213:T88NXO102K
122:ChemSpider
86:3D model (
65:CAS Number
170:213-083-5
162:EC Number
75:922-67-8
358:Density
180:PubChem
469:
418:methyl
400:is an
342:84.074
286:SMILES
31:Names
421:ester
261:InChI
193:13536
131:12948
88:JSmol
467:ISBN
204:UNII
459:doi
423:of
230:EPA
183:CID
488::
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412:CH
408:CO
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414:3
410:2
406:2
330:2
327:O
324:4
321:H
318:4
315:C
232:)
228:(
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