
2-Bromo-4-cyanophenol | CAS:2315-86-8
2-Bromo-4-cyanophenol
- Name:2-Bromo-4-cyanophenol
- CAS:2315-86-8
- Synonyms:3-Bromo-4-hydroxybenzonitrile
- Molecular Formula:C7H4BrNO
- Molecular Weight:198.02
- EINESC:219-022-9
Description
Properties
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Safety
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SDS
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Alfa-Aesar | View & Download |
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Apollo | View & Download |
Synthetic Route
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More
Articles
Peer-Reviewed Papers
Identification and characterization of a mandelamide hydrolase and an NAD(P)+-dependent benzaldehyde dehydrogenase from Pseudomonas putida ATCC 12633.Michael J McLeish et al.Journal of bacteriology, 185(8), 2451-2456 (2003-04-03)
Metabolic engineering of Escherichia coli for the production of benzoic acid from glucose.Zi Wei Luo et al.Metabolic engineering, 62, 298-311 (2020-10-18)
Synthesis and fungicidal activity of N-2-(3-methoxy-4-propargyloxy)phenethyl amides. Part II: anti-oomycetic mandelamides.Clemens Lamberth et al.Pest management science, 62(5), 446-451 (2006-03-22)
[Molecular biology aspects of the antimicrobial effect of synthetic chemotherapeutic agents].N Popov Zeitschrift fur arztliche Fortbildung, 76(15), 662-666 (1982-08-01)
Synthesis and fungicidal activity of N-2-(3-methoxy-4-propargyloxy) phenethyl amides. Part 3: stretched and heterocyclic mandelamide oomyceticides.Clemens Lamberth et al.Pest management science, 63(1), 57-62 (2006-11-02)
The mandelamide keto-enol system in aqueous solution. Generation of the enol by hydration of phenylcarbamoylcarbene.Y Chiang et al.Journal of the American Chemical Society, 125(1), 187-194 (2003-01-08)
Using directed evolution to probe the substrate specificity of mandelamide hydrolase.Pan-Fen Wang et al.Protein engineering, design & selection : PEDS, 22(2), 103-110 (2008-12-17)
Catalytic asymmetric addition of dimethylzinc to alpha-ketoesters, using mandelamides as ligands.Gonzalo Blay et al.Organic letters, 8(7), 1287-1290 (2006-03-28)
Anisotropic and hydrogen bonding effects in phenylglyoxamides and mandelamides: theoretical and NMR conformational evaluation.Biank T Gonçalves et al.Magnetic resonance in chemistry : MRC, 46(5), 418-426 (2008-03-11)
Identification of amino acid residues responsible for the enantioselectivity and amide formation capacity of the Arylacetonitrilase from Pseudomonas fluorescens EBC191.Christoph Kiziak et al.Applied and environmental microbiology, 75(17), 5592-5599 (2009-07-08)
Specificity and mechanism of mandelamide hydrolase catalysis.S A Adediran et al.Archives of biochemistry and biophysics, 618, 23-31 (2017-01-29)
Remarks
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Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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