184006-13-1 Usage
Description
[2-(2-Azido-ethoxy)-ethoxy]-acetaldehyde is a chemical compound characterized by its molecular formula C6H11N3O3. It is a derivative of acetaldehyde, featuring two ethoxy groups and an azido group. [2-(2-Azido-ethoxy)-ethoxy]-acetaldehyde is recognized for its role in the synthesis of a variety of organic compounds and serves as a crucial building block in the preparation of polymers and materials. Given its potentially explosive nature, it is classified as a hazardous chemical, necessitating adherence to proper handling and storage protocols. Furthermore, it holds significant potential for applications in the realms of organic chemistry and materials science.
Uses
Used in Organic Synthesis:
[2-(2-Azido-ethoxy)-ethoxy]-acetaldehyde is utilized as a key intermediate in the synthesis of various organic compounds. Its unique structure, which includes the azido group and ethoxy groups, allows for a wide range of reactions and the creation of diverse chemical products.
Used in Polymer and Material Preparation:
[2-(2-Azido-ethoxy)-ethoxy]-acetaldehyde also serves as a building block in the preparation of polymers and materials. Its incorporation into these systems can lead to the development of novel materials with specific properties tailored for various applications.
Used in Chemical Research:
Given its structural features and reactivity, [2-(2-Azido-ethoxy)-ethoxy]-acetaldehyde is a valuable compound for research in the field of organic chemistry. It can be used to study reaction mechanisms, explore new synthetic routes, and investigate the properties of newly synthesized compounds.
Used in Materials Science:
In the field of materials science, [2-(2-Azido-ethoxy)-ethoxy]-acetaldehyde may find applications in the development of new materials with specific characteristics. Its integration into material systems could result in the creation of materials with enhanced properties, such as improved mechanical strength, thermal stability, or chemical resistance.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, the compound's potential reactivity and structural diversity may also make it a candidate for use in the pharmaceutical industry. It could be employed in the development of new drugs or drug delivery systems, taking advantage of its unique properties to target specific biological processes or improve the efficacy of existing medications.
Used in Hazardous Chemical Handling and Storage:
Given its classification as a hazardous chemical, [2-(2-Azido-ethoxy)-ethoxy]-acetaldehyde also has implications for the chemical industry in terms of handling and storage. Companies and research facilities working with this compound must adhere to strict safety protocols to minimize the risk of accidents and ensure the safe use of the compound in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 184006-13-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,0,0 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 184006-13:
(8*1)+(7*8)+(6*4)+(5*0)+(4*0)+(3*6)+(2*1)+(1*3)=111
111 % 10 = 1
So 184006-13-1 is a valid CAS Registry Number.
184006-13-1Relevant articles and documents
CONJUGATES COMPRISING SELF-IMMOLATIVE GROUPS AND METHODS RELATED THERETO
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Page/Page column 94, (2017/06/27)
In some aspects, the invention relates to an antibody-drug conjugate, comprising an antibody; a linker; and an active agent. The antibody-drug conjugate may comprise a self- immolative group. The linker may comprise an O-substituted oxime, e.g., wherein the oxygen atom of the oxime is substituted with a group that covalently links the oxime to the active agent; and the carbon atom of the oxime is substituted with a group that covalently links the oxime to the antibody.
Liposome-like fucopeptides as sialyl Lewis X mimetics
Lin, Chun-Cheng,Kimura, Teiji,Wu, Shih-Hsiung,Weitz-Schmidt, Gabriele,Wong, Chi-Huey
, p. 2755 - 2760 (2007/10/03)
Several fucodipeptides and their liposome-like derivatives were prepared and tested as inhibitors of sialyl Lewis X binding to E-selectin. It has been found that trans-hydroxyproline (D or L) can be used to mimic the galactose residue of sialyl Lewis X, and the mimetic containing 3,4-dihydroxy-D-proline is the most active with IC50 value (50 μM) 10-fold greater than sialyl Lewis X. Derivatization of a hydroxythreonine-containing fucodipeptides into a covalent liposome-like derivative, however, provides a mimetic with only IC50 ~ 30 μM.
