Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C4H10O2 |
| Molecular Weight | 90.121 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(C)CO
InChI
InChIKey=YTTFFPATQICAQN-UHFFFAOYSA-N
InChI=1S/C4H10O2/c1-4(3-5)6-2/h4-5H,3H2,1-2H3
| Molecular Formula | C4H10O2 |
| Molecular Weight | 90.121 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Palladium-catalyzed isobenzofuran generation under neutral conditions via oxidative addition to lactol methyl ether. | 2002 Oct 3 |
|
| Investigations on the subchronic toxicity of 2-methoxypropanol-1(acetate) in rats. | 2005 Feb |
|
| Acute effects of an exposure to 100 ppm 1-methoxypropanol-2 on the upper airways of human subjects. | 2013 Jul 4 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:46:25 GMT 2023
by
admin
on
Sat Dec 16 09:46:25 GMT 2023
|
| Record UNII |
18B570XOYF
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
1589-47-5
Created by
admin on Sat Dec 16 09:46:25 GMT 2023 , Edited by admin on Sat Dec 16 09:46:25 GMT 2023
|
PRIMARY | |||
|
18B570XOYF
Created by
admin on Sat Dec 16 09:46:25 GMT 2023 , Edited by admin on Sat Dec 16 09:46:25 GMT 2023
|
PRIMARY | |||
|
14846
Created by
admin on Sat Dec 16 09:46:25 GMT 2023 , Edited by admin on Sat Dec 16 09:46:25 GMT 2023
|
PRIMARY | |||
|
18B570XOYF
Created by
admin on Sat Dec 16 09:46:25 GMT 2023 , Edited by admin on Sat Dec 16 09:46:25 GMT 2023
|
PRIMARY | |||
|
2380833
Created by
admin on Sat Dec 16 09:46:25 GMT 2023 , Edited by admin on Sat Dec 16 09:46:25 GMT 2023
|
PRIMARY | |||
|
216-455-5
Created by
admin on Sat Dec 16 09:46:25 GMT 2023 , Edited by admin on Sat Dec 16 09:46:25 GMT 2023
|
PRIMARY |