CAS 79-15-2
:N-Bromoacetamide
Description:
N-Bromoacetamide is an organic compound characterized by its bromo and acetamide functional groups. It appears as a white to off-white crystalline solid and is soluble in water and various organic solvents. The compound is known for its reactivity, particularly as a brominating agent in organic synthesis. N-Bromoacetamide can release bromine in aqueous solutions, making it useful in various chemical reactions, including the bromination of alkenes and aromatic compounds. It is also employed in biochemical applications, such as protein labeling and modification. The compound has a relatively low toxicity profile, but safety precautions should be taken when handling it, as it can be irritating to the skin and eyes. Additionally, N-Bromoacetamide is often stored in a cool, dry place to maintain its stability and prevent decomposition. Overall, its unique properties and reactivity make it a valuable reagent in both synthetic and analytical chemistry.
Formula:C2H4BrNO
InChI:InChI=1/C2H4BrNO/c1-2(5)4-3/h1H3,(H,4,5)
InChI key:InChIKey=VBTQNRFWXBXZQR-UHFFFAOYSA-N
SMILES:C(NBr)(C)=O
Synonyms:- Acetamide, N-bromo-
- Acetobromamide
- Ccris 4590
- N-Bromoacetamide
- NBA
- n-bromo-acetamid
- N-BROMOACETAMIDE (NBA)
- NBAAcetobromamide
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Found 6 products.
N-Bromoacetamide
CAS:Formula:C2H4BrNOPurity:>97.0%(T)Color and Shape:White to Orange to Green powder to crystalMolecular weight:137.96N-Bromoacetamide, 95%
CAS:<p>Abolishes the rapid inactivation of membrane sodium- and potassium-ion channels. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code</p>Formula:C2H4BrNOPurity:95%Color and Shape:White to pale cream to cream to yellow, Crystals or powder or crystalline powder or fused solidMolecular weight:137.96N-Bromoacetamide
CAS:<p>N-Bromoacetamide is a reactive chemical that can react with the sodium channel to produce a postulated effect. It has been shown to inhibit the kinetics of the sodium channel in whole-cell voltage clamp experiments. This inhibition is reversible and does not depend on the pH of the solution. Bromoacetamide has been shown to have an irreversible inhibition on potassium channels, which may be due to its ability to form covalent bonds with sulfhydryl groups. Bromoacetamide also inhibits voltage-gated calcium channels, but at a slower rate than it does for sodium channels. N-Bromoacetamide has been shown to be effective in pharmacological treatments for epilepsy, myasthenia gravis, and multiple sclerosis.</p>Formula:C2H4BrNOPurity:Min. 95%Color and Shape:PowderMolecular weight:137.96 g/mol





