Weight | 226.114 g/mol |
---|---|
Formula | C7H16BrNO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
Acetylcholine bromide (66-23-9)
Acetylcholine · Acetylcholine Chloride · Miochol
Score:
#1217 in Neuroscience
,
#5216 in Biology
,
#6840 in Chemistry
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- The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine. (Nature, 1980)
- Paradoxical Vasoconstriction Induced by Acetylcholine in Atherosclerotic Coronary Arteries (The New England Journal of Medicine, 1986)
- Atomic structure of acetylcholinesterase from Torpedo californica: a prototypic acetylcholine-binding protein (Science, 1991)
- Nicotinic acetylcholine receptor |[alpha]|7 subunit is an essential regulator of inflammation (Nature, 2002)
- THE REACTION OF ACETYLCHOLINE AND OTHER CARBOXYLIC ACID DERIVATIVES WITH HYDROXYLAMINE, AND ITS ANALYTICAL APPLICATION (Journal of Biological Chemistry, 1949)
- Refined Structure of the Nicotinic Acetylcholine Receptor at 4A Resolution (Journal of Molecular Biology, 2005)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Acetylcholine
- Acetylcholine Chloride
- Miochol
- Acetylcholine Iodide
- Acetylcholine Picrate
- Acetylcholine Fluoride
- Acetilcolina Cusi
- Acetylcholine Hydroxide
- Chloroacetylcholine
- Bromoacetylcholine
- Acetylcholine Picrate (1:1)
- 2-(Acetyloxy)-N,N,N-trimethylethanaminium
- Acetylcholine Perchlorate
- Acetylcholine Sulfate (1:1)
- Acetylcholine L-Tartrate
- Acetylcholine L Tartrate
-
SMILESCC(=O)OCC[N+](C)(C)C.[Br-]
-
InChIKeyZEHGKSPCAMLJDC-UHFFFAOYSA-M
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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