Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H14O |
| Molecular Weight | 114.1855 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1CCCCC1
InChI
InChIKey=GHDIHPNJQVDFBL-UHFFFAOYSA-N
InChI=1S/C7H14O/c1-8-7-5-3-2-4-6-7/h7H,2-6H2,1H3
| Molecular Formula | C7H14O |
| Molecular Weight | 114.1855 |
| 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 |
|---|---|---|
| Calcium-promoted catalytic degradation of PCDDs, PCDFs, and coplanar PCBs under a mild wet process. | 2006-03-15 |
|
| Intrinsic conformational preferences of substituted cyclohexanes and tetrahydropyrans evaluated at the CCSD(T) complete basis set limit: implications for the anomeric effect. | 2005-12-08 |
|
| Intramolecular syn and anti hydrosilylation and silicon-assisted cross-coupling: highly regio- and stereoselective synthesis of trisubstituted allylic alcohols. | 2003-04-03 |
|
| Studies in bicyclo[3.1.0]hexane methanolysis. Ring opening of activated cyclopropanes under acidic and basic conditions. | 2002-09-06 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:52:51 GMT 2025
by
admin
on
Mon Mar 31 19:52:51 GMT 2025
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| Record UNII |
I340UAT8HB
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID10239268
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