Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H9O.BF4 |
| Molecular Weight | 147.908 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[O+](C)C.F[B-](F)(F)F
InChI
InChIKey=CZVZBKHWOFJNCR-UHFFFAOYSA-N
InChI=1S/C3H9O.BF4/c1-4(2)3;2-1(3,4)5/h1-3H3;/q+1;-1
| Molecular Formula | BF4 |
| Molecular Weight | 86.805 |
| Charge | -1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C3H9O |
| Molecular Weight | 61.103 |
| Charge | 1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| The tetrodotoxin binding site is within the outer vestibule of the sodium channel. | 2010-02-01 |
|
| New automated and high-throughput quantitative analysis of urinary ketones by multifiber exchange-solid phase microextraction coupled to fast gas chromatography/negative chemical-electron ionization/mass spectrometry. | 2010 |
|
| Mechanisms of cascade reactions in the syntheses of camptothecin-family alkaloids: intramolecular [4(+) + 2] reactions of N-arylimidates and alkynes. | 2009-11-19 |
|
| Interaction of selective amino acid residues of K(ca) channels with carbon monoxide. | 2003-05 |
|
| Synthesis and characterization of the first examples of perfluoroalkyl-substituted trialkyloxonium salts, [(CH3)2OCF3]+[Sb2F11]- and [(CH3)2OCF(CF3)2]+[Sb2F11]-. | 2001-08-13 |
|
| The reaction of protonated dimethyl ether with dimethyl ether: temperature and isotope effects on the methyl cation transfer reaction forming trimethyloxonium cation and methanol. | 2001-05-02 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 20:02:40 GMT 2025
by
admin
on
Tue Apr 01 20:02:40 GMT 2025
|
| Record UNII |
BFC3NMU8S8
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
2735153
Created by
admin on Tue Apr 01 20:02:40 GMT 2025 , Edited by admin on Tue Apr 01 20:02:40 GMT 2025
|
PRIMARY | |||
|
420-37-1
Created by
admin on Tue Apr 01 20:02:40 GMT 2025 , Edited by admin on Tue Apr 01 20:02:40 GMT 2025
|
PRIMARY | |||
|
m11159
Created by
admin on Tue Apr 01 20:02:40 GMT 2025 , Edited by admin on Tue Apr 01 20:02:40 GMT 2025
|
PRIMARY | |||
|
206-994-4
Created by
admin on Tue Apr 01 20:02:40 GMT 2025 , Edited by admin on Tue Apr 01 20:02:40 GMT 2025
|
PRIMARY | |||
|
BFC3NMU8S8
Created by
admin on Tue Apr 01 20:02:40 GMT 2025 , Edited by admin on Tue Apr 01 20:02:40 GMT 2025
|
PRIMARY | |||
|
Trimethyloxonium tetrafluoroborate
Created by
admin on Tue Apr 01 20:02:40 GMT 2025 , Edited by admin on Tue Apr 01 20:02:40 GMT 2025
|
PRIMARY | |||
|
DTXSID20883377
Created by
admin on Tue Apr 01 20:02:40 GMT 2025 , Edited by admin on Tue Apr 01 20:02:40 GMT 2025
|
PRIMARY | |||
|
528455
Created by
admin on Tue Apr 01 20:02:40 GMT 2025 , Edited by admin on Tue Apr 01 20:02:40 GMT 2025
|
PRIMARY |