Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H14O3 |
| Molecular Weight | 158.195 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C(=O)OC(=O)C(C)C
InChI
InChIKey=LSACYLWPPQLVSM-UHFFFAOYSA-N
InChI=1S/C8H14O3/c1-5(2)7(9)11-8(10)6(3)4/h5-6H,1-4H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| A catalytic one-step process for the chemo- and regioselective acylation of monosaccharides. | 2007-10-24 |
|
| Reliable and fast quantitative analysis of active ingredient in pharmaceutical suspension using Raman spectroscopy. | 2007-06-12 |
|
| A new non-invasive, quantitative Raman technique for the determination of an active ingredient in pharmaceutical liquids by direct measurement through a plastic bottle. | 2007-03-28 |
|
| New reliable Raman collection system using the wide area illumination (WAI) scheme combined with the synchronous intensity correction standard for the analysis of pharmaceutical tablets. | 2006-10-10 |
|
| New class of pyridine catalyst having a conformation switch system: asymmetric acylation of various sec-alcohols. | 2006-09-01 |
|
| Steric effects in the uncatalyzed and DMAP-catalyzed acylation of alcohols-quantifying the window of opportunity in kinetic resolution experiments. | 2006-07-24 |
|
| Kinetics of gelation and thermal sensitivity of N-isobutyryl chitosan hydrogels. | 2005-09-13 |
|
| Kinetic resolution of allylic alcohols using a chiral phosphine catalyst. | 2001-02-22 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
202-603-6
Created by
admin on Mon Mar 31 21:05:53 GMT 2025 , Edited by admin on Mon Mar 31 21:05:53 GMT 2025
|
PRIMARY | |||
|
DTXSID7026609
Created by
admin on Mon Mar 31 21:05:53 GMT 2025 , Edited by admin on Mon Mar 31 21:05:53 GMT 2025
|
PRIMARY | |||
|
97-72-3
Created by
admin on Mon Mar 31 21:05:53 GMT 2025 , Edited by admin on Mon Mar 31 21:05:53 GMT 2025
|
PRIMARY | |||
|
84261
Created by
admin on Mon Mar 31 21:05:53 GMT 2025 , Edited by admin on Mon Mar 31 21:05:53 GMT 2025
|
PRIMARY | |||
|
5309
Created by
admin on Mon Mar 31 21:05:53 GMT 2025 , Edited by admin on Mon Mar 31 21:05:53 GMT 2025
|
PRIMARY | |||
|
N85A80FJDT
Created by
admin on Mon Mar 31 21:05:53 GMT 2025 , Edited by admin on Mon Mar 31 21:05:53 GMT 2025
|
PRIMARY | |||
|
7346
Created by
admin on Mon Mar 31 21:05:53 GMT 2025 , Edited by admin on Mon Mar 31 21:05:53 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD
