D-Galactose, 6-azido-6-deoxy-


Chemical Name: D-Galactose, 6-azido-6-deoxy-
CAS Number: 66927-03-5
Product Number: AG003N35(AGN-PC-0OFXNI)
Synonyms:
MDL No:
Molecular Formula: C6H11N3O5
Molecular Weight: 205.16864

Identification/Properties


Properties
Storage:
-10 ℃;
Computed Properties
Molecular Weight:
205.17g/mol
XLogP3:
-1.8
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
6
Exact Mass:
205.07g/mol
Monoisotopic Mass:
205.07g/mol
Topological Polar Surface Area:
112A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
230
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


NMR Spectrum


Other Analytical Data


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Chemical Structure



6-Azido-6-deoxy-D-galactose, also known as 6-azido-6-deoxygalactose or 6-azido-Gal, is a versatile compound widely utilized in chemical synthesis for various purposes. In the field of organic chemistry, 6-Azido-6-deoxy-D-galactose is commonly employed as a chemical building block in the preparation of complex carbohydrates and glycoconjugates.One key application of 6-Azido-6-deoxy-D-galactose is its use as a precursor in click chemistry reactions, specifically copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC). The azido group present in 6-azido-Gal can undergo a highly efficient and bioorthogonal reaction with alkynes in the presence of a copper catalyst, enabling the site-specific and selective modification of biomolecules and synthetic materials.Additionally, 6-Azido-6-deoxy-D-galactose can be utilized for the synthesis of azido-functionalized carbohydrates, glycoconjugates, and glycomimetics. By incorporating the azido group into the carbohydrate structure, researchers can introduce chemical handles for further conjugation reactions or bioorthogonal labeling studies. This compound's ability to functionalize and modify carbohydrates makes it a valuable tool in glycobiology research and drug development.In summary, 6-Azido-6-deoxy-D-galactose plays a crucial role in chemical synthesis, particularly in the construction of complex carbohydrates and glycoconjugates through click chemistry reactions. Its versatility and compatibility with bioorthogonal chemistry make it a valuable reagent for researchers in various fields, including organic chemistry, glycobiology, and pharmaceutical sciences.