Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C6H11NO2 |
| Molecular Weight | 129.157 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)[C@@H]1CCCN1
InChI
InChIKey=BLWYXBNNBYXPPL-YFKPBYRVSA-N
InChI=1S/C6H11NO2/c1-9-6(8)5-3-2-4-7-5/h5,7H,2-4H2,1H3/t5-/m0/s1
| Molecular Formula | C6H11NO2 |
| Molecular Weight | 129.157 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Inclusion complexes of 2-chloroethylnitrososulfamides (CENS) with beta-cyclodextrin. | 2004 Jan |
|
| Stereoselective synthesis of a potent thrombin inhibitor by a novel P2-P3 lactone ring opening. | 2004 May 28 |
|
| Kinetic determination of potassium affinities by IRMPD: elucidation of precursor ion structures. | 2009 Jul 9 |
|
| Dynamic kinetic resolution of N-benzoyl-DL-amino acids via peptide bond forming reactions. | 2010 Apr |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:58:28 GMT 2023
by
admin
on
Sat Dec 16 08:58:28 GMT 2023
|
| Record UNII |
0II79F4L0K
|
| Record Status |
Validated (UNII)
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| Record Version |
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219-932-6
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853477
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0II79F4L0K
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2577-48-2
Created by
admin on Sat Dec 16 08:58:28 GMT 2023 , Edited by admin on Sat Dec 16 08:58:28 GMT 2023
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| Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |
