Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H5FO |
| Molecular Weight | 124.1124 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
FC(=O)C1=CC=CC=C1
InChI
InChIKey=HPMLGNIUXVXALD-UHFFFAOYSA-N
InChI=1S/C7H5FO/c8-7(9)6-4-2-1-3-5-6/h1-5H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Beta-fluoroamphetamines via the stereoselective synthesis of benzylic fluorides. | 2010-07-02 |
|
| Isothiourea-mediated stereoselective C-acylation of silyl ketene acetals. | 2010-06-04 |
|
| Enantioselective ring opening of epoxides by fluoride anion promoted by a cooperative dual-catalyst system. | 2010-03-17 |
|
| Corrrelation of the specific rates of solvolysis of ethyl fluoroformate using the extended Grunwald-Winstein equation. | 2009-03 |
|
| Electrolytic partial fluorination of organic compounds. 79. Anodic fluorination of spiropyrazoline-5,3'-chroman-4-ones and thiochromanone analogues. A route to aroyl fluoride derivatives. | 2005-09-16 |
|
| Correlation of the rates of solvolysis of benzoyl fluoride and a consideration of leaving-group effects. | 2004-10-15 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
67999
Created by
admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
|
PRIMARY | |||
|
DTXSID5060019
Created by
admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
|
PRIMARY | |||
|
455-32-3
Created by
admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
|
PRIMARY | |||
|
LOR25I34HD
Created by
admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
|
PRIMARY | |||
|
207-244-9
Created by
admin on Mon Mar 31 19:09:58 GMT 2025 , Edited by admin on Mon Mar 31 19:09:58 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD
