Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H4Br2 |
| Molecular Weight | 199.872 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
BrCC(Br)=C
InChI
InChIKey=YMFWYDYJHRGGPF-UHFFFAOYSA-N
InChI=1S/C3H4Br2/c1-3(5)2-4/h1-2H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Formal synthesis of (+/-)-platensimycin. | 2007-04-26 |
|
| Identification of glutathione conjugates of 2, 3-dibromopropene in male ICR mice. | 2006-02 |
|
| Novel carbonyl bromoallylation/Heck reaction sequence. Stereocontrolled access to bicyclic beta-lactams. | 2005-04-01 |
|
| Straightforward asymmetric entry to highly functionalized 3-substituted 3-hydroxy-beta-lactams via Baylis-Hillman or bromoallylation reactions. | 2004-02-06 |
|
| Haloalkane dehalogenase LinB from Sphingomonas paucimobilis UT26: X-ray crystallographic studies of dehalogenation of brominated substrates. | 2003-09-02 |
|
| Controlling chemoselectivity in vinyl and allylic C-X bond activation with palladium catalysis: a pK(a)-based electronic switch. | 2002-02-20 |
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8DNE7K7Z6P
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513-31-5
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m4300
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6200
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SUBSTANCE RECORD
