Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H10O3 |
| Molecular Weight | 118.1311 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(CO)C(O)=O
InChI
InChIKey=RDFQSFOGKVZWKF-UHFFFAOYSA-N
InChI=1S/C5H10O3/c1-5(2,3-6)4(7)8/h6H,3H2,1-2H3,(H,7,8)
| Molecular Formula | C5H10O3 |
| Molecular Weight | 118.1311 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Joint experimental and theoretical studies of the mechanism for the gas phase elimination kinetics of methyl 2,2-dimethyl-3-hydroxypropionate. | 2009-04-16 |
|
| A concise method for the preparation of peptide and arginine-rich peptide-conjugated antisense oligonucleotide. | 2003-05-22 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:24:58 GMT 2025
by
admin
on
Mon Mar 31 19:24:58 GMT 2025
|
| Record UNII |
BJP2CXK56P
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
78548
Created by
admin on Mon Mar 31 19:24:58 GMT 2025 , Edited by admin on Mon Mar 31 19:24:58 GMT 2025
|
PRIMARY | |||
|
BJP2CXK56P
Created by
admin on Mon Mar 31 19:24:58 GMT 2025 , Edited by admin on Mon Mar 31 19:24:58 GMT 2025
|
PRIMARY | |||
|
DTXSID4063616
Created by
admin on Mon Mar 31 19:24:58 GMT 2025 , Edited by admin on Mon Mar 31 19:24:58 GMT 2025
|
PRIMARY | |||
|
225-419-8
Created by
admin on Mon Mar 31 19:24:58 GMT 2025 , Edited by admin on Mon Mar 31 19:24:58 GMT 2025
|
PRIMARY | |||
|
115936
Created by
admin on Mon Mar 31 19:24:58 GMT 2025 , Edited by admin on Mon Mar 31 19:24:58 GMT 2025
|
PRIMARY | |||
|
4835-90-9
Created by
admin on Mon Mar 31 19:24:58 GMT 2025 , Edited by admin on Mon Mar 31 19:24:58 GMT 2025
|
PRIMARY |