Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C7H14O2 |
| Molecular Weight | 130.1849 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)OCC1CO1
InChI
InChIKey=SFJRUJUEMVAZLM-UHFFFAOYSA-N
InChI=1S/C7H14O2/c1-7(2,3)9-5-6-4-8-6/h6H,4-5H2,1-3H3
| Molecular Formula | C7H14O2 |
| Molecular Weight | 130.1849 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Novel microbial epoxide hydrolases for biohydrolysis of glycidyl derivatives. | 2005 Dec 6 |
|
| Purification and characterisation of a novel enantioselective epoxide hydrolase from Aspergillus niger M200. | 2006 Feb |
|
| Cloning of an epoxide hydrolase-encoding gene from Aspergillus niger M200, overexpression in E. coli, and modification of activity and enantioselectivity of the enzyme by protein engineering. | 2007 Oct 15 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:03:33 GMT 2023
by
admin
on
Sat Dec 16 09:03:33 GMT 2023
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| Record UNII |
35F8X83D0G
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID4024692
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24314
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35F8X83D0G
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231-640-0
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7665-72-7
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| Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
