Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H8O |
| Molecular Weight | 84.1164 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CCC[C@]1([H])O2
InChI
InChIKey=GJEZBVHHZQAEDB-SYDPRGILSA-N
InChI=1S/C5H8O/c1-2-4-5(3-1)6-4/h4-5H,1-3H2/t4-,5+
| Molecular Formula | C5H8O |
| Molecular Weight | 84.1164 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| An experimental and computational study of 1,2-hydrogen migrations in 2-hydroxycyclopentylidene and its conjugate base. | 2001 Mar 9 |
|
| New catalysts for the base-promoted isomerization of epoxides to allylic alcohols. Broadened scope and near-perfect asymmetric induction. | 2002 Mar 8 |
|
| Influence of microemulsions on enantioselective synthesis of (R)-cyclopent-2-enol catalyzed by vitamin B12. | 2006 Jun 6 |
|
| Enol formation and ring-opening in OH-initiated oxidation of cycloalkenes. | 2008 Dec 25 |
|
| Determination of the structure of cyclopentene oxide and the argon-cyclopentene oxide van der Waals complex. | 2010 Jan 28 |
|
| Manipulating the stereoselectivity of limonene epoxide hydrolase by directed evolution based on iterative saturation mutagenesis. | 2010 Nov 10 |
|
| Amino-alcohol ligands: synthesis and structure of N,N'-bis(2-hydroxycyclopentyl)ethane-1,2-diamine and its salts, and an assessment of its fitness and that of related ligands for complexing metal ions. | 2010 Sep 6 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 07:55:11 GMT 2023
by
admin
on
Sat Dec 16 07:55:11 GMT 2023
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| Record UNII |
U3EKO505C5
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| Record Status |
Validated (UNII)
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| Record Version |
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