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6-AZIDO-6-DEOXY-D-GALACTOSE, also known as 6-azido-galactose or 6-azido-gal, is a synthetic carbohydrate derivative that features an azido group. 6-AZIDO-6-DEOXY-D-GALACTOSE is widely recognized for its role in chemical biology and bioconjugation studies. Its unique ability to selectively label glycoconjugates and glycoproteins through copper-catalyzed azide-alkyne cycloaddition, commonly referred to as click chemistry, positions it as an indispensable tool in the realms of glycobiology and bioorthogonal chemistry.

66927-03-5

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66927-03-5 Usage

Uses

Used in Chemical Biology:
6-AZIDO-6-DEOXY-D-GALACTOSE is used as a selective labeling agent for glycoconjugates and glycoproteins, enabling researchers to study the structure and function of these biomolecules in various biological processes.
Used in Bioconjugation Studies:
6-AZIDO-6-DEOXY-D-GALACTOSE is used as a key component in click chemistry, facilitating the efficient and specific conjugation of biomolecules for applications such as drug delivery, imaging, and the development of biosensors.
Used in the Study of Glycosylation Pathways:
6-AZIDO-6-DEOXY-D-GALACTOSE is used as a research tool to investigate the biosynthesis and regulation of glycans, which are crucial for numerous cellular functions and are often implicated in diseases.
Used in the Development of Glycoengineering Techniques:
6-AZIDO-6-DEOXY-D-GALACTOSE is used as a building block in the creation of novel glycoconjugates with tailored properties, contributing to advances in the field of glycoengineering.
Used in the Investigation of Glycan-Protein Interactions:
6-AZIDO-6-DEOXY-D-GALACTOSE is used to probe and understand the intricate interactions between glycans and proteins, which are vital for many physiological and pathological processes.
Used in Pharmaceutical Development:
6-AZIDO-6-DEOXY-D-GALACTOSE is used as a component in the design and synthesis of new drugs targeting glycan-related diseases, potentially leading to innovative therapeutics.
Used in Diagnostics:
6-AZIDO-6-DEOXY-D-GALACTOSE is used in the development of diagnostic tools that rely on the specific recognition of glycan structures, aiding in the detection and monitoring of various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 66927-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,2 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66927-03:
(7*6)+(6*6)+(5*9)+(4*2)+(3*7)+(2*0)+(1*3)=155
155 % 10 = 5
So 66927-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H11N3O5/c7-9-8-1-3(11)5(13)6(14)4(12)2-10/h2-6,11-14H,1H2/t3-,4+,5+,6-/m1/s1

66927-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-AZIDO-6-DEOXY-D-GALACTOSE

1.2 Other means of identification

Product number -
Other names -

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:66927-03-5 SDS

66927-03-5Upstream product

66927-03-5Downstream Products

66927-03-5Relevant academic research and scientific papers

Hydroxyazepanes as inhibitors of glycosidase and HIV protease

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, (2011/05/18)

Hydroxyazepanes display inhibitory activity with respect to glycosidase, with Kivalues from-moderate to low micromolar range. Benzyl and 3,6-dibenzyl derivatives of hydroxyazepanes display inhibitory activity with respect to HIV protease. These compounds are synthesized either by chemoenzymatic or chemical methodologies.

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