Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H18O2 |
| Molecular Weight | 170.2487 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(CCC=C(C)C)CC(O)=O
InChI
InChIKey=GJWSUKYXUMVMGX-UHFFFAOYSA-N
InChI=1S/C10H18O2/c1-8(2)5-4-6-9(3)7-10(11)12/h5,9H,4,6-7H2,1-3H3,(H,11,12)
| Molecular Formula | C10H18O2 |
| Molecular Weight | 170.2487 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Environmental concentrations of methoprene and its transformation products after the treatment of Altosid® XR Briquets in the city of Richmond, British Columbia, Canada. | 2010-10 |
|
| Fumigant toxicity of essential oils to the German cockroach (Dictyoptera: Blattellidae). | 2010-06 |
|
| Topical toxicity of essential oils to the German cockroach (Dictyoptera: Blattellidae). | 2010-04 |
|
| Oxidation of citronellal to citronellic acid by molecular oxygen using supported gold catalysts. | 2008 |
|
| Efficacy of botanical extracts from Callitris glaucophylla, against Aedes aegypti and Culex annulirostris mosquitoes. | 2006-12 |
|
| Methylcrotonyl-CoA and geranyl-CoA carboxylases are involved in leucine/isovalerate utilization (Liu) and acyclic terpene utilization (Atu), and are encoded by liuB/liuD and atuC/atuF, in Pseudomonas aeruginosa. | 2005-11 |
|
| Utilization of geraniol is dependent on molybdenum in Pseudomonas aeruginosa: evidence for different metabolic routes for oxidation of geraniol and citronellol. | 2005-07 |
|
| Malate:quinone oxidoreductase (MqoB) is required for growth on acetate and linear terpenes in Pseudomonas citronellolis. | 2005-05-01 |
|
| Inhibition of citrus postharvest pathogens by vapor of citral and related compounds in culture. | 2003-04-23 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:36:52 GMT 2025
by
admin
on
Mon Mar 31 18:36:52 GMT 2025
|
| Record UNII |
1JJT408R87
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
207-939-7
Created by
admin on Mon Mar 31 18:36:52 GMT 2025 , Edited by admin on Mon Mar 31 18:36:52 GMT 2025
|
PRIMARY | |||
|
DTXSID1047106
Created by
admin on Mon Mar 31 18:36:52 GMT 2025 , Edited by admin on Mon Mar 31 18:36:52 GMT 2025
|
PRIMARY | |||
|
SUB183872
Created by
admin on Mon Mar 31 18:36:52 GMT 2025 , Edited by admin on Mon Mar 31 18:36:52 GMT 2025
|
PRIMARY | |||
|
502-47-6
Created by
admin on Mon Mar 31 18:36:52 GMT 2025 , Edited by admin on Mon Mar 31 18:36:52 GMT 2025
|
PRIMARY | |||
|
80507
Created by
admin on Mon Mar 31 18:36:52 GMT 2025 , Edited by admin on Mon Mar 31 18:36:52 GMT 2025
|
PRIMARY | |||
|
1230
Created by
admin on Mon Mar 31 18:36:52 GMT 2025 , Edited by admin on Mon Mar 31 18:36:52 GMT 2025
|
PRIMARY | |||
|
1JJT408R87
Created by
admin on Mon Mar 31 18:36:52 GMT 2025 , Edited by admin on Mon Mar 31 18:36:52 GMT 2025
|
PRIMARY | |||
|
100000170109
Created by
admin on Mon Mar 31 18:36:52 GMT 2025 , Edited by admin on Mon Mar 31 18:36:52 GMT 2025
|
PRIMARY | |||
|
10402
Created by
admin on Mon Mar 31 18:36:52 GMT 2025 , Edited by admin on Mon Mar 31 18:36:52 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
