73018-98-1

Basic information

• Product Name: AZIDOGLYCEROL
• Synonyms: 3-AZIDOGLYCEROL;3-AZIDO-1,2-PROPANEDIOL;1,2-Propanediol, 3-azido-;Ccris 2062
• CAS NO: 73018-98-1
• Molecular Formula: C₃H₇N₃O₂
• Molecular Weight: 117.13
• Mol File: 73018-98-1.mol
• Article Data: 19

Chemical Properties

• Appearance: /
• CAS DataBase Reference: AZIDOGLYCEROL(CAS DataBase Reference)
• NIST Chemistry Reference: AZIDOGLYCEROL(73018-98-1)
• EPA Substance Registry System: AZIDOGLYCEROL(73018-98-1)

Safety Data

• Hazardous Substances Data: 73018-98-1(Hazardous Substances Data)

Usage

Safety Profile

Mutation data reported. Whenheated to decomposition it emits toxic vapors of NOx.

InChI:InChI=1/C3H7N3O2/c4-6-5-1-3(8)2-7/h3,7-8H,1-2H2

Upstream product

• 556-52-5 oxiranyl-methanol 
• 96-24-2 3-monochloro-1,2-propanediol 
• 25261-56-7 4-(azidomethyl)-2,2?dimethyl-1,3-dioxolane 

Downstream Products

• 168431-73-0 1-azido-3-(p-toluenesulfonyloxy)propan-2-ol 
• 96800-65-6 <3-(4-acetylphenyl)-2-oxo-5-oxazolidinyl>methyl azide 
• 367925-74-4 5-azidomethyl-3-phenyl-1,3-oxazolidin-2-one 
• 1044255-51-7 C₁₈H₂₂N₄O₅S 
• 1015479-94-3 4-(azidomethyl)-2-(3-methoxyphenyl)-1,3-dioxolane 
• 1015479-89-6 4-(azidomethyl)-2-(2-chlorophenyl)-1,3-dioxolane 
• 1015479-90-9 4-(azidomethyl)-2-(3-chlorophenyl)-1,3-dioxolane 
• 1015479-91-0 4-(azidomethyl)-2-(4-chlorophenyl)-1,3-dioxolane 

Relevant articles and documents

Turning Off Transcription with Bacterial RNA Polymerase through CuAAC Click Reactions of DNA Containing 5-Ethynyluracil

Copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) click reaction in the major groove of DNA containing 5-ethynyluracil (UE) with azides was used for turning off sequence-specific protein–DNA interactions. The concept was first demonstrated

Hydrophilic Clicked 2,6-Bis-Triazolyl-pyridines Endowed with High Actinide Selectivity and Radiochemical Stability: Toward a Closed Nuclear Fuel Cycle

There is still an evident need for selective and stable ligands able to separate actinide(III) from lanthanide(III) metal ions in view of the treatment of the accumulated radioactive waste and of the recycling of minor actinides. We have herein demonstrated that hydrophilic 2,6-bis-Triazolyl-pyridines are able to strip all actinides in all the different oxidation states from a diglycolamide-containing kerosene solution into an acidic aqueous phase. The ascertained high actinide selectivity, efficiency, extraction kinetics, and chemical/radiolytic stability spotlight this hydrophilic class of ligands as exceptional candidates for advanced separation processes fundamental for closing the nuclear fuel cycle and solving the environmental issues related to the management of existing nuclear waste.

IONIC LIQUIDS, AND THE METHOD FOR PREPARING THE SAME AND THE METHOD FOR SYNTHESIZING 2-AZIDOALCOHOL USING THE SAME

The present invention provides a method of preparing a room temperature ionic liquid (RTIL), comprising: a precursor forming step of forming a trimesylate by using glycerol as a starting material; and a step of obtaining a reactant by mixing the precursor