| Weight | 179.057 g/mol |
|---|---|
| Formula | C6H11BrO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
1-Bromopinacolone (5469-26-1)
1-bromo-2-pinacolone
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- Reactions of 1-bromo-2-[14C]pinacolone with acetylcholinesterase from Torpedo nobiliana. Effects of 5-trimethylammonio-2-pentanone and diisopropyl fluorophosphate. (Biochimica et Biophysica Acta, 1989)
- 1-Bromopinacolone, an active site-directed covalent inhibitor for acetylcholinesterase. (Journal of Biological Chemistry, 1982)
- Labeling of cysteine 231 in acetylcholinesterase from Torpedo nobiliana by the active-site directed reagent, 1-bromo-2-[14C] pinacolone. Effects of 2,2'-dipyridyl disulfide and other sulfhydryl reagents. (Journal of Biological Chemistry, 1993)
- Active-site peptides of acetylcholinesterase of Electrophorus electricus: labelling of His-440 by 1-bromo-[2-14C]pinacolone and Ser-200 by tritiated diisopropyl fluorophosphate (Biochimica et Biophysica Acta, 1994)
- Labeling by 1-bromo-2-14C-Pinacolone of His-440 and Trp-435 in Acetylcholinesterase from Electrophorous Electricus. (1993)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1-bromo-2-pinacolone
-
SMILESCC(C)(C)C(=O)CBr
-
InChIKeySAIRZMWXVJEBMO-UHFFFAOYSA-N
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Alternate Names
External Links
Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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(3393-64-4)
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Pivalamide
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CYCLOBUTANONE
(1191-95-3)
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2,3-butanedione
(431-03-8)
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3 suppliers
2-Methyl-4-pentenal
(5187-71-3)
2 alternate names
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2-Hexanone-1,1,1,3,3-d5
(4840-82-8)
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2,6-Dimethyl-4-heptanone
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3 suppliers
calcium 3-methyl-2-oxobutanoate
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3-(1-Adamantyl)-3-oxopropanenitrile
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1-cyclopentylpropan-1-one
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2-Bromo-2-methylpropionyl bromide
(20769-85-1)
2 alternate names
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2-Bromobutyryl bromide
(26074-52-2)
2 alternate names
3 suppliers
1-Bromopinacolone
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