Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H10ClN2 |
| Molecular Weight | 133.599 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 1 |
SHOW SMILES / InChI
SMILES
CN1CC[N+](C)=C1Cl
InChI
InChIKey=DMIXJRHWHHYJOX-UHFFFAOYSA-N
InChI=1S/C5H10ClN2/c1-7-3-4-8(2)5(7)6/h3-4H2,1-2H3/q+1
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
| Name | Type | Language | ||
|---|---|---|---|---|
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Preferred Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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C2T502SBK1
Created by
admin on Mon Mar 31 19:48:11 GMT 2025 , Edited by admin on Mon Mar 31 19:48:11 GMT 2025
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PRIMARY | |||
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4176750
Created by
admin on Mon Mar 31 19:48:11 GMT 2025 , Edited by admin on Mon Mar 31 19:48:11 GMT 2025
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PRIMARY | |||
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75126-82-8
Created by
admin on Mon Mar 31 19:48:11 GMT 2025 , Edited by admin on Mon Mar 31 19:48:11 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD
