Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H10ClN2.Cl |
| Molecular Weight | 169.052 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Cl-].CN1CC[N+](C)=C1Cl
InChI
InChIKey=AEBBXVHGVADBHA-UHFFFAOYSA-M
InChI=1S/C5H10ClN2.ClH/c1-7-3-4-8(2)5(7)6;/h3-4H2,1-2H3;1H/q+1;/p-1
| Molecular Formula | C5H10ClN2 |
| Molecular Weight | 133.599 |
| Charge | 1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| 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 |
|---|---|---|
| One-step conversion of unprotected sugars to beta-glycosyl azides using 2-chloroimidazolinium salt in aqueous solution. | 2009-06-21 |
|
| Synthetic studies on macroviracin A: a rapid construction of C(42) macrocyclic dilactone corresponding to the core. | 2004-06-25 |
|
| Structure assignment, total synthesis, and evaluation of the phosphatase modulating activity of glucolipsin A. | 2004-01-23 |
|
| Structure assignment, total synthesis, and antiviral evaluation of cycloviracin B1. | 2003-10-29 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:12:00 GMT 2025
by
admin
on
Mon Mar 31 20:12:00 GMT 2025
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| Record UNII |
56KA2A1U1D
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| Record Status |
Validated (UNII)
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| Record Version |
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