Details
Stereochemistry | RACEMIC |
Molecular Formula | C10H20O |
Molecular Weight | 156.2652 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(CCCC(C)(C)O)C=C
InChI
InChIKey=XSNQECSCDATQEL-UHFFFAOYSA-N
InChI=1S/C10H20O/c1-5-9(2)7-6-8-10(3,4)11/h5,9,11H,1,6-8H2,2-4H3
Molecular Formula | C10H20O |
Molecular Weight | 156.2652 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Reversible unfolding of bovine odorant binding protein induced by guanidinium hydrochloride at neutral pH. | 2002 Sep 23 |
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Unfolding and refolding of porcine odorant binding protein in guanidinium hydrochloride: equilibrium studies at neutral pH. | 2003 Dec 1 |
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Analysis of insecticidal Azadirachta indica A. Juss. fractions. | 2004 Jan-Feb |
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Rhodiolosides A-E, monoterpene glycosides from Rhodiola rosea. | 2006 Aug |
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Cleaning products and air fresheners: emissions and resulting concentrations of glycol ethers and terpenoids. | 2006 Jun |
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Evaluation of the developmental toxicity of dihydromyrcenol in rats. | 2009 Mar-Apr |
|
Fragrance material review on dihydromyrcenol. | 2010 Jan |
|
Dynamic solid phase microextraction sampling for reactive terpenes in the presence of ozone. | 2010 Oct 15 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:46:41 GMT 2023
by
admin
on
Fri Dec 15 15:46:41 GMT 2023
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Record UNII |
46L1B02ND9
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Record Status |
Validated (UNII)
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Record Version |
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1659907
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29096
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46L1B02ND9
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242-362-4
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100000174910
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C542861
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DTXSID8029317
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