Details
Stereochemistry | RACEMIC |
Molecular Formula | C5H11HgN2O2.Cl |
Molecular Weight | 367.2 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Cl-].COC(C[Hg+])CNC(N)=O
InChI
InChIKey=BJFGVYCULWBXKF-UHFFFAOYSA-M
InChI=1S/C5H11N2O2.ClH.Hg/c1-4(9-2)3-7-5(6)8;;/h4H,1,3H2,2H3,(H3,6,7,8);1H;/q;;+1/p-1
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 |
Molecular Formula | C5H11HgN2O2 |
Molecular Weight | 331.74 |
Charge | 1 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Chlormerodrin: clinical effectiveness and absence of toxicity in congestive heart failure; report of a four-year study. | 1959 Apr 4 |
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EFFECTS OF CHLORMERODRIN, P-CHLOROMERCURIBENZOATE AND DICHLORPHENAMIDE ON RENAL SODIUM REABSORPTION AND OXYGEN CONSUMPTION. | 1964 |
|
COMPARATIVE STUDIES ON MERCURATED 1-, 3-, AND 5- ALLYLHYDANTOINS AND CHLORMERODRIN. | 1964 Jun 1 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 14:59:16 GMT 2023
by
admin
on
Fri Dec 15 14:59:16 GMT 2023
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Record UNII |
99T5TWO621
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C448
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Code System | Code | Type | Description | ||
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Chlormerodrin
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DB00534
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99T5TWO621
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m3375
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PRIMARY | Merck Index | ||
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2716
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CHEMBL2110562
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C65315
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200-530-4
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446
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4911
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59445
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62-37-3
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SUB06184MIG
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D002717
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100000081563
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19911
Created by
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |