2-Bromoacetamide
2-Bromoacetamide structure
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Common Name | 2-Bromoacetamide | ||
|---|---|---|---|---|
| CAS Number | 683-57-8 | Molecular Weight | 137.963 | |
| Density | 1.8±0.1 g/cm3 | Boiling Point | 271.6±23.0 °C at 760 mmHg | |
| Molecular Formula | C2H4BrNO | Melting Point | 87-91 °C(lit.) | |
| MSDS | USA | Flash Point | 118.1±22.6 °C | |
| Symbol |
GHS05, GHS06 |
Signal Word | Danger | |
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Carborane-derived local anesthetics are isomer dependent.
ChemMedChem 10(1) , 62-7, (2014) Clinically there is a need for local anesthetics with a greater specificity of action on target cells and longer duration. We have synthesized a series of local anesthetic derivatives we call boronicaines in which the aromatic phenyl ring of lidocaine was rep... |
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(N)-methanocarba 2,N6-disubstituted adenine nucleosides as highly potent and selective A3 adenosine receptor agonists.
J. Med. Chem. 48(6) , 1745-58, (2005) A series of ring-constrained (N)-methanocarba-5'-uronamide 2,N(6)-disubstituted adenine nucleosides have been synthesized via Mitsunobu condensation of the nucleobase precursor with a pseudosugar ring containing a 5'-ester functionality. Following appropriate... |
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Kinetic analysis of sequence-specific alkylation of DNA by pyrimidine oligodeoxyribonucleotide-directed triple-helix formation.
Bioconjug. Chem. 8(3) , 354-64, (1997) Attachment of a nondiffusible bromoacetyl electrophile to the 5-position of a thymine at the 5'-end of a pyrimidine oligodeoxyribonucleotide affords sequence-specific alkylation of a guanine base in duplex DNA two base pairs to the 5'-side of a local triple-h... |
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Targeting renal dipeptidase (dehydropeptidase I) for inactivation by mechanism-based inactivators.
J. Med. Chem. 34 , 1914, (1991)
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