Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H7ClO |
| Molecular Weight | 94.54 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOCCl
InChI
InChIKey=FCYRSDMGOLYDHL-UHFFFAOYSA-N
InChI=1S/C3H7ClO/c1-2-5-3-4/h2-3H2,1H3
| Molecular Formula | C3H7ClO |
| Molecular Weight | 94.54 |
| 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 |
|---|---|---|
| Synthesis of novel uracil non-nucleoside derivatives as potential reverse transcriptase inhibitors of HIV-1. | 2009-11 |
|
| Expedient syntheses of the N-heterocyclic carbene precursor imidazolium salts IPr.HCl, IMes.HCl and IXy.HCl. | 2007-08-28 |
|
| Unexpected formation of hydroxybiphenylmethane derivatives and some new observations on Labat test. | 2006-10 |
|
| Synthesis of non-nucleosides: 7- and 1,3-substituents of new pyrrolo[2,3-d]pyrimidin-4-ones on antiviral activity. | 2006-04 |
|
| Synthesis of 2-(aminocarbonylmethylthio)-1H-imidazoles as novel Capravirine analogues. | 2005-07-01 |
|
| Synthesis of 2-methylsulfanyl-1H-imidazoles as novel non-nucleoside reverse transcriptase inhibitors (NNRTIs). | 2003-06 |
|
| bis(Chloromethyl) ether and technical-grade chloromethyl methyl ether. | 2002 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:22:52 GMT 2025
by
admin
on
Mon Mar 31 22:22:52 GMT 2025
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| Record UNII |
08T7N64Z04
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| Record Status |
Validated (UNII)
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| Record Version |
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18523
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3188-13-4
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