Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H9ClO |
| Molecular Weight | 108.567 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)OCl
InChI
InChIKey=IXZDIALLLMRYOU-UHFFFAOYSA-N
InChI=1S/C4H9ClO/c1-4(2,3)6-5/h1-3H3
| Molecular Formula | C4H9ClO |
| Molecular Weight | 108.567 |
| 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 |
|---|---|---|
| 5α-Dihydro-vespertilin acetate. | 2010-02-13 |
|
| Utilization of N-X bonds in the synthesis of N-heterocycles. | 2009-08-18 |
|
| Aziridination of C60 with simple amides and catalytic rearrangement of the aziridinofullerenes to azafulleroids. | 2009-02-20 |
|
| Synthesis of sulfonimidamides from sulfinamides by oxidation with N-chlorosuccinimide. | 2007-09-25 |
|
| Oxidative rearrangement of indoles: a new approach to the EFHG-tetracyclic core of diazonamide A. | 2007-04-13 |
|
| Preparation and reactivity of [D3d]-octahedrane: the most stable (CH)12 hydrocarbon. | 2005-10-21 |
|
| Cyclic sulfonimidates by dynamic diastereomer-differentiating cyclisation: large-scale synthesis and mechanistic studies. | 2001-03-16 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:56:38 GMT 2025
by
admin
on
Mon Mar 31 19:56:38 GMT 2025
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| Record UNII |
LS2JTI16JZ
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| Record Status |
Validated (UNII)
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| Record Version |
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