Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H12O |
| Molecular Weight | 100.1589 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1CCCC1
InChI
InChIKey=SKTCDJAMAYNROS-UHFFFAOYSA-N
InChI=1S/C6H12O/c1-7-6-4-2-3-5-6/h6H,2-5H2,1H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Enhancement of enzyme activity and enantioselectivity by cyclopentyl methyl ether in the transesterification catalyzed by Pseudomonas cepacia lipase co-lyophilized with cyclodextrins. | 2005 Mar |
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| Practical and robust method for regio- and stereoselective preparation of (E)-ketene tert-butyl TMS acetals and beta-ketoester-derived tert-butyl (1Z,3E)-1,3-bis(TMS)dienol ethers. | 2007 Oct 12 |
|
| 2-Methoxycyclopentyl analogues of a Pseudomonas aeruginosa quorum sensing modulator. | 2008 Jun |
|
| Recycling the tert-butanesulfinyl group in the synthesis of amines using tert-butanesulfinamide. | 2009 Apr 3 |
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138539
Created by
admin on Sat Dec 16 03:46:19 GMT 2023 , Edited by admin on Sat Dec 16 03:46:19 GMT 2023
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4067E5GBKB
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admin on Sat Dec 16 03:46:19 GMT 2023 , Edited by admin on Sat Dec 16 03:46:19 GMT 2023
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Cyclopentyl methyl ether
Created by
admin on Sat Dec 16 03:46:19 GMT 2023 , Edited by admin on Sat Dec 16 03:46:19 GMT 2023
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5614-37-9
Created by
admin on Sat Dec 16 03:46:19 GMT 2023 , Edited by admin on Sat Dec 16 03:46:19 GMT 2023
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DTXSID2074958
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admin on Sat Dec 16 03:46:19 GMT 2023 , Edited by admin on Sat Dec 16 03:46:19 GMT 2023
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m4012
Created by
admin on Sat Dec 16 03:46:19 GMT 2023 , Edited by admin on Sat Dec 16 03:46:19 GMT 2023
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PRIMARY | Merck Index |
SUBSTANCE RECORD
