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Sku CI23011_250_MG
Chem Impex
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Product Information

Product Name
p-Azidophenacyl bromide
Brand Name
Chem Impex
Product Number
23011
CAS
57018-46-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
92627
IUPAC Name
1-(4-azidophenyl)-2-bromoethanone
InChI Key
LZJPDRANSVSGOR-UHFFFAOYSA-N
SMILES
C1=CC(=CC=C1C(=O)CBr)N=N+=N-

Application

p-Azidophenacyl bromide is widely utilized in research focused on:

Bioconjugation: This compound is often used to attach biomolecules, such as proteins or nucleic acids, to surfaces or other molecules, facilitating the development of targeted drug delivery systems.

Photochemistry: It serves as a photosensitive compound in various photochemical reactions, allowing researchers to study light-induced processes and develop new materials with unique properties.

Medicinal Chemistry: p-Azidophenacyl bromide is important in synthesizing potential pharmaceutical agents, particularly in the design of inhibitors or probes for biological studies.

Material Science: This chemical is utilized in the development of polymeric materials that respond to light, enhancing the functionality of coatings or films used in electronics and optics.

Analytical Chemistry: It plays a role in the development of analytical methods, such as fluorescence labeling, which aids in the detection and quantification of various biological samples.

References

Uncaging Antisense Oligonucleotides with Small Molecules

Publication Name: Synfacts
Publication Date: 2022-01-18
DOI: 10.1055/s-0041-1737249

Synthesis, antimicrobial activity, and determination of the lipophilicity of ((cyclohex-3-enylmethylene)hydrazinyl)thiazole derivatives

Publication Name: Medicinal Chemistry Research
Publication Date: 2019-09-09
DOI: 10.1007/s00044-019-02433-2

YpeB dimerization may be required to stabilize SleB for effective germination of Bacillus anthracis spores

Publication Name: BMC Microbiology
Publication Date: 2019-07-26
DOI: 10.1186/s12866-019-1544-1

Thiazoles with cyclopropyl fragment as antifungal, anticonvulsant, and anti-Toxoplasma gondii agents: synthesis, toxicity evaluation, and molecular docking study

Publication Name: Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents
Publication Date: 2018-07-21
DOI: 10.1007/s00044-018-2221-x

INO80 exchanges H2A.Z for H2A by translocating on DNA proximal to histone dimers

Publication Name: Nature Communications
Publication Date: 2017-06-12
DOI: 10.1038/ncomms15616