Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H12O |
| Molecular Weight | 100.1589 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)C(C)C
InChI
InChIKey=HYTRYEXINDDXJK-UHFFFAOYSA-N
InChI=1S/C6H12O/c1-4-6(7)5(2)3/h5H,4H2,1-3H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis of 2H-1,2-benzothiazine 1,1-dioxides via heteroannulation reactions of 2-iodobenzenesulfonamide with ketone enolates under S(RN)1 conditions. | 2005 Nov 11 |
|
| Charge separation distance for flexible donor-bridge-acceptor systems after electron-transfer quenching. | 2008 Aug 21 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
Ethyl isopropyl ketone
Created by
admin on Fri Dec 15 19:34:50 GMT 2023 , Edited by admin on Fri Dec 15 19:34:50 GMT 2023
|
PRIMARY | |||
|
11265
Created by
admin on Fri Dec 15 19:34:50 GMT 2023 , Edited by admin on Fri Dec 15 19:34:50 GMT 2023
|
PRIMARY | |||
|
0R392X5X26
Created by
admin on Fri Dec 15 19:34:50 GMT 2023 , Edited by admin on Fri Dec 15 19:34:50 GMT 2023
|
PRIMARY | |||
|
565-69-5
Created by
admin on Fri Dec 15 19:34:50 GMT 2023 , Edited by admin on Fri Dec 15 19:34:50 GMT 2023
|
PRIMARY | |||
|
209-288-4
Created by
admin on Fri Dec 15 19:34:50 GMT 2023 , Edited by admin on Fri Dec 15 19:34:50 GMT 2023
|
PRIMARY | |||
|
DTXSID2073196
Created by
admin on Fri Dec 15 19:34:50 GMT 2023 , Edited by admin on Fri Dec 15 19:34:50 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
