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4-AZIDOPHENYLACRYLALDEHYDE, with the molecular formula C9H7N3O, is a yellow solid chemical compound that serves as a versatile reagent in organic synthesis and a precursor for the production of various organic compounds. Its unique structure, featuring both an azide and an aldehyde functional group, makes it a valuable building block for the synthesis of a wide range of molecules. Known for its participation in cycloaddition reactions, especially with alkynes, 4-AZIDOPHENYLACRYLALDEHYDE is instrumental in the preparation of azide-modified biomolecules and polymers. Furthermore, it holds potential in the development of photoactivatable crosslinkers and fluorescent probes for biological studies, making it a significant compound in the realm of organic chemistry.

22736-78-3

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22736-78-3 Usage

Uses

Used in Organic Synthesis:
4-AZIDOPHENYLACRYLALDEHYDE is used as a reagent in organic synthesis for its ability to participate in cycloaddition reactions, particularly with alkynes, facilitating the creation of diverse molecular structures.
Used in the Production of Azide-Modified Biomolecules and Polymers:
In the field of biochemistry, 4-AZIDOPHENYLACRYLALDEHYDE is utilized as a precursor to produce azide-modified biomolecules and polymers, which are essential for various biological and medical applications.
Used in the Development of Photoactivatable Crosslinkers:
4-AZIDOPHENYLACRYLALDEHYDE is employed as a component in the development of photoactivatable crosslinkers, which are crucial for studying protein-protein interactions and other biological processes in a controlled manner.
Used in the Creation of Fluorescent Probes for Biological Studies:
4-AZIDOPHENYLACRYLALDEHYDE is also used in the creation of fluorescent probes, which are vital for visualizing and tracking biological processes at the molecular level, enhancing our understanding of cellular mechanisms.
Used in Research and Development:
4-AZIDOPHENYLACRYLALDEHYDE is utilized in research and development settings for its potential applications in advancing the fields of chemistry and biology, particularly in the synthesis of new compounds and the study of biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 22736-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,3 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22736-78:
(7*2)+(6*2)+(5*7)+(4*3)+(3*6)+(2*7)+(1*8)=113
113 % 10 = 3
So 22736-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H7N3O/c10-12-11-9-5-3-8(4-6-9)2-1-7-13/h1-7H

22736-78-3 Well-known Company Product Price

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  • TCI America

  • (A0971)  4-Azidocinnamaldehyde  >98.0%(HPLC)

  • 22736-78-3

  • 5g

  • 1,420.00CNY

  • Detail

22736-78-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-azidophenyl)prop-2-enal

1.2 Other means of identification

Product number -
Other names 4-Azidocinnamaldehyde

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22736-78-3 SDS

22736-78-3Downstream Products

22736-78-3Relevant academic research and scientific papers

Novel cinnamaldehyde compound having an azido group

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Page/Page column 2, (2008/06/13)

The invention provides a novel azidocinnamaldehyde compound which, when used as an intermediate for providing a photosensitive moiety of a photoresist, introduces a photosensitive moiety having high sensitivity and attaining high contrast between the expo

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