Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H5N3O.ClH |
| Molecular Weight | 135.552 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.NNC(=O)CC#N
InChI
InChIKey=CEOVDOULQCPTMU-UHFFFAOYSA-N
InChI=1S/C3H5N3O.ClH/c4-2-1-3(7)6-5;/h1,5H2,(H,6,7);1H
| Molecular Formula | C3H5N3O |
| Molecular Weight | 99.0913 |
| Charge | 0 |
| 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 |
DescriptionSources: https://www.rlsnet.ru/mnn_index_id_1940.htm
Sources: https://www.rlsnet.ru/mnn_index_id_1940.htm
Cyacetacide is a biochemical used in the past as an anti-tuberculosis agent and currently used in Russia to for the treatment of various forms of tubercular lesions of the eye: keratitis, scleritis, uveitis, chorioretinitis, tuberculosis-allergic diseases and eye diseases of non-tubercular origin. Cyacetacide has also been used to derive compounds that may have antitumor properties.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:21:44 GMT 2025
by
admin
on
Mon Mar 31 22:21:44 GMT 2025
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| Record UNII |
8W5485PW3E
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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12235876
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5897-13-2
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m3940
Created by
admin on Mon Mar 31 22:21:44 GMT 2025 , Edited by admin on Mon Mar 31 22:21:44 GMT 2025
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PRIMARY | Merck Index | ||
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8W5485PW3E
Created by
admin on Mon Mar 31 22:21:44 GMT 2025 , Edited by admin on Mon Mar 31 22:21:44 GMT 2025
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PRIMARY |