| Identification | Back Directory | [Name]
2-BROMO-5-CYANO-4-PICOLINE | [CAS]
1003711-35-0 | [Synonyms]
2-BROMO-5-CYANO-4-PICOLINE
6-broMo-4-Methylnicotinonitrile
6-bromo-4-methylpyridine-3-carbonitrile
6-Bromo-4-methyl-3-pyridinecarbonitrile
3-Pyridinecarbonitrile, 6-bromo-4-methyl- | [EINECS(EC#)]
125-856-9 | [Molecular Formula]
C7H5BrN2 | [MDL Number]
MFCD09839265 | [MOL File]
1003711-35-0.mol | [Molecular Weight]
197.03 |
| Chemical Properties | Back Directory | [Boiling point ]
288℃ | [density ]
1.61 | [Fp ]
128℃ | [storage temp. ]
Inert atmosphere,2-8°C | [pka]
-2.00±0.18(Predicted) | [InChI]
InChI=1S/C7H5BrN2/c1-5-2-7(8)10-4-6(5)3-9/h2,4H,1H3 | [InChIKey]
DHUDYHHQMIRPHS-UHFFFAOYSA-N | [SMILES]
C1=NC(Br)=CC(C)=C1C#N |
| Questions And Answer | Back Directory | [Application]
6-Bromo-4-methylpyridin-3-carboxynitrile can be used to prepare substituted nitrogen-containing heterocyclic compounds that can be used as inhibitors of ROMK channel activity. Multiple pieces of evidence indicate that inhibition of ROMK channel activity leads to urinary sodium excretion, diuresis, and a decrease in blood pressure. Therefore, ROMK inhibition may provide a novel mechanism for blood pressure regulation and diuresis in patients with hypertension, congestive heart failure, or any other edematous conditions. |
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