| Weight | 137.964 g/mol |
|---|---|
| Formula | C2H4BrNO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
n-bromoacetamide (79-15-2)
Score:
#1619 in Physics
,
#1812 in Biochemistry
,
#3948 in Biology
,
#4968 in Chemistry
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- Effect of N-bromoacetamide on single sodium channel currents in excised membrane patches. (The Journal of General Physiology, 1982)
- The Use of N-Bromosuccinimide and N-Bromoacetamide for the Selective Cleavage of C-Tryptophyl Peptide Bonds in Model Peptides and Glucagon1 (Journal of the American Chemical Society, 1960)
- Statistical analysis of single sodium channels. Effects of N-bromoacetamide (Biophysical Journal, 1984)
- NBromoacetamideA New Nitrogen Source for the Catalytic Asymmetric Aminohydroxylation of Olefins (Angewandte Chemie, 1997)
- Removal of sodium channel inactivation in squid giant axons by n-bromoacetamide. (The Journal of General Physiology, 1978)
- N-bromoacetamide removes a calcium-dependent component of channel opening from calcium-activated potassium channels in rat skeletal muscle. (The Journal of General Physiology, 1985)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=O)NBr
-
InChIKeyVBTQNRFWXBXZQR-UHFFFAOYSA-N
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