14999-44-1

Basic information

• Product Name: 2-amino-2-deoxy-D-glucose hydroiodide
• Synonyms: 2-amino-2-deoxy-D-glucose hydroiodide
• CAS NO: 14999-44-1
• Molecular Formula: C6H14INO5
• Molecular Weight: 307.08353
• EINECS: 239-089-8
• Mol File: 14999-44-1.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 449.9°Cat760mmHg
• Flash Point: 225.9°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 5.53E-10mmHg at 25°C
• CAS DataBase Reference: 2-amino-2-deoxy-D-glucose hydroiodide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-2-deoxy-D-glucose hydroiodide(14999-44-1)
• EPA Substance Registry System: 2-amino-2-deoxy-D-glucose hydroiodide(14999-44-1)

Safety Data

• Hazardous Substances Data: 14999-44-1(Hazardous Substances Data)

Usage

Description

2-amino-2-deoxy-D-glucose hydroiodide is a chemical compound derived from glucose, a simple sugar, featuring both an amino group and a hydroxyl group. It is commonly utilized as a reagent in organic and biochemistry, serving as a building block for complex chemical structures and playing a significant role in the synthesis and development of carbohydrate-based drugs and pharmaceuticals. 2-amino-2-deoxy-D-glucose hydroiodide is typically presented as a white to off-white solid powder, and due to its potential toxicity, it requires careful handling.

Uses

Used in Organic Chemistry:
2-amino-2-deoxy-D-glucose hydroiodide is used as a reagent for the synthesis of various organic molecules, contributing to the creation of more complex chemical structures due to its unique functional groups.
Used in Biochemistry:
In biochemistry, 2-amino-2-deoxy-D-glucose hydroiodide is employed in the study and development of carbohydrate-based drugs and pharmaceuticals, leveraging its structural properties to enhance drug design and therapeutic applications.
Used in Pharmaceutical Development:
2-amino-2-deoxy-D-glucose hydroiodide is used as a building block in the pharmaceutical industry for the development of new drugs, particularly those targeting carbohydrate-related biological processes, due to its ability to mimic and interact with natural sugars in biological systems.
Used in Research:
In academic and research settings, 2-amino-2-deoxy-D-glucose hydroiodide is utilized as a tool to investigate the roles and interactions of sugars in biological systems, aiding in the understanding of carbohydrate biochemistry and its implications in health and disease.

InChI:InChI=1/C6H13NO5.HI/c7-3-5(10)4(9)2(1-8)12-6(3)11;/h2-6,8-11H,1,7H2;1H/t2-,3-,4-,5-,6-;/m1./s1