Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H8O |
| Molecular Weight | 84.1164 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(O)C#C
InChI
InChIKey=CEBKHWWANWSNTI-UHFFFAOYSA-N
InChI=1S/C5H8O/c1-4-5(2,3)6/h1,6H,2-3H3
| Molecular Formula | C5H8O |
| Molecular Weight | 84.1164 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Basic reactivity of CaO: investigating active sites under operating conditions. | 2010-11-28 |
|
| 4-(4-Meth-oxy-phen-yl)-2-methyl-but-3-yn-2-ol. | 2010-06-30 |
|
| 4,4'-[2,5-Bis(dodec-yloxy)-p-phenyl-ene]bis-(2-methyl-but-3-yn-2-ol). | 2010-06-05 |
|
| 9-Isopropenyl-4-methyl-2H-thieno[2,3-h]chromen-2-one. | 2009-05-20 |
|
| 2,2'-Dimethyl-4,4'-(sulfonyldi-p-phenyl-ene)dibut-3-yn-2-ol dihydrate. | 2009-01-08 |
|
| 4-(9-Anthryl)-2-methylbutyn-2-ol. | 2008-01-23 |
|
| Ligand accelerated indium(III)-catalyzed asymmetric alkynylation of aldehydes with 2-methyl-3-butyn-2-ol as an ethyne equivalent donor. | 2007-03-07 |
|
| Hydride-alkenylcarbyne to alkenylcarbene transformation in bisphosphine-osmium complexes. | 2005-08-10 |
|
| Tandem Sonogashira coupling: an efficient tool for the synthesis of diarylalkynes. | 2004-12-23 |
|
| Six- and eightfold palladium-catalyzed cross-coupling reactions of hexa- and octabromoarenes. | 2004-12-17 |
|
| Regioselective synthesis of 6-alkyl- and 6-prenylpolyhydroxyisoflavones and 6-alkylcoumaronochromone derivatives. | 2004-11 |
|
| Synthesis, X-ray crystal structure and biological properties of acetylenic flavone derivatives. | 2003-09 |
|
| One step Pd(0)-catalyzed synthesis, X-ray analysis, and photophysical properties of cyclopent[hi]aceanthrylene: fullerene-like properties in a nonalternant cyclopentafused aromatic hydrocarbon. | 2002-01-09 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:40:33 GMT 2025
by
admin
on
Mon Mar 31 21:40:33 GMT 2025
|
| Record UNII |
EHB904XHKH
|
| Record Status |
Validated (UNII)
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| Record Version |
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Systematic Name | English | ||
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Preferred Name | English | ||
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| Code System | Code | Type | Description | ||
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m7378
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204-070-5
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115-19-5
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C015352
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8258
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DTXSID2021949
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523
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2-Methylbut-3-yn-2-ol
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EHB904XHKH
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admin on Mon Mar 31 21:40:33 GMT 2025 , Edited by admin on Mon Mar 31 21:40:33 GMT 2025
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PRIMARY |