Details
Stereochemistry | ACHIRAL |
Molecular Formula | C3H5BrO |
Molecular Weight | 136.975 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)CBr
InChI
InChIKey=VQFAIAKCILWQPZ-UHFFFAOYSA-N
InChI=1S/C3H5BrO/c1-3(5)2-4/h2H2,1H3
Molecular Formula | C3H5BrO |
Molecular Weight | 136.975 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
4-(2-aminooxyethoxy)-2-(ethylureido)quinoline-oligonucleotide conjugates: synthesis, binding interactions, and derivatization with peptides. | 2003 Mar-Apr |
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A novel formal total synthesis of cephalotaxine. | 2005 Apr 15 |
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13C NMR, infrared, solvation and theoretical investigation of the conformational isomerism in 1-haloacetones (X = Cl, Br and I). | 2005 Jul |
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Metabolism and disposition of 1-bromopropane in rats and mice following inhalation or intravenous administration. | 2006 Aug 15 |
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Propargyl bromide as an excellent alpha-bromoacetone equivalent: convenient and new route to alpha-aroylacetones. | 2006 Jan 6 |
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Halogenated acetaldehydes: analysis, stability and fate in drinking water. | 2006 Jul |
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Hydroxyl-radical-initiated oxidation mechanism of bromopropane. | 2008 Aug 28 |
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Transient receptor potential ankyrin 1 antagonists block the noxious effects of toxic industrial isocyanates and tear gases. | 2009 Apr |
|
Bromido(2,2':6',2''-terpyridine)platinum(II) dibromidoaurate(I) dimethyl sulfoxide solvate. | 2009 Aug 26 |
|
Disinfection by-product formation and mutagenic assay caused by preozonation of groundwater containing bromide. | 2009 Nov |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 01:25:35 GMT 2023
by
admin
on
Sat Dec 16 01:25:35 GMT 2023
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Record UNII |
3O8L0EWR5Q
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Record Status |
Validated (UNII)
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Record Version |
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209-928-2
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C018235
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598-31-2
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m2678
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11715
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315
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BROMOACETONE
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DTXSID6060507
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3O8L0EWR5Q
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51845
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