Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H16 |
| Molecular Weight | 124.2233 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCC#C
InChI
InChIKey=OSSQSXOTMIGBCF-UHFFFAOYSA-N
InChI=1S/C9H16/c1-3-5-7-9-8-6-4-2/h1H,4-9H2,2H3
| Molecular Formula | C9H16 |
| Molecular Weight | 124.2233 |
| 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 |
|---|---|---|
| Adducts of thianthrene- and phenoxathiin cation radical tetrafluoroborates to 1-alkynes. Structures and formation of 1-(5-thianthreniumyl)- and 1-(10-phenoxathiiniumyl)alkynes on alumina leading to alpha-ketoylides and alpha-ketols. | 2005 Nov 25 |
|
| An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation. | 2007 Oct 29 |
|
| [Comparative study of the anatomic and clinical effect of Weaver or subtotal subscapularis tendon section in Latarjet procedure]. | 2008 Feb |
|
| De novo asymmetric synthesis of cladospolide B-D: structural reassignment of cladospolide D via the synthesis of its enantiomer. | 2009 Mar 5 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:01:49 GMT 2023
by
admin
on
Fri Dec 15 18:01:49 GMT 2023
|
| Record UNII |
760V9GP5A1
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| Record Status |
Validated (UNII)
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| Record Version |
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760V9GP5A1
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admin on Fri Dec 15 18:01:49 GMT 2023 , Edited by admin on Fri Dec 15 18:01:49 GMT 2023
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