Details
Stereochemistry | RACEMIC |
Molecular Formula | C11H14BrN2O3.Na |
Molecular Weight | 325.134 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].CC(C)C1(CC(Br)=C)C(=O)[N-]C(=O)N(C)C1=O
InChI
InChIKey=OJFQAJVRMVQQHN-UHFFFAOYSA-M
InChI=1S/C11H15BrN2O3.Na/c1-6(2)11(5-7(3)12)8(15)13-10(17)14(4)9(11)16;/h6H,3,5H2,1-2,4H3,(H,13,15,17);/q;+1/p-1
Molecular Formula | C11H15BrN2O3 |
Molecular Weight | 303.152 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Molecular Formula | Na |
Molecular Weight | 22.9898 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Enibomal (narcobarbital) is a barbiturate drug. By its chemical structure, it is N-methylated derivative of propallynolal. Narcobarbital was discovered in 1930s and later investigated as an anesthetic agent in gynecological surgery and electroconvulsive treatment. In the United States, narcobarbital is classified as a schedule III drug and is not found in pharmaceutical preparations. In Europe, narcobarbital was used in veterinary as a general anesthetic for pigs, but by 2000 it was withdrawn and no longer available at the market.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:46:24 GMT 2023
by
admin
on
Fri Dec 15 19:46:24 GMT 2023
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Record UNII |
M2BUZ8YH0F
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Record Status |
Validated (UNII)
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3329-16-6
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100000079481
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C010308
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23691019
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DTXSID50954928
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M2BUZ8YH0F
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m837
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DBSALT002515
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SUB13673MIG
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222-050-4
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |