57011-48-0

Basic information

• Product Name: 1,3-DIAZIDO-2-PROPANOL
• CAS NO: 57011-48-0
• Molecular Formula: C₃H₆N₆O
• Molecular Weight: 142.12
• Mol File: 57011-48-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3-DIAZIDO-2-PROPANOL (CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-DIAZIDO-2-PROPANOL (57011-48-0)
• EPA Substance Registry System: 1,3-DIAZIDO-2-PROPANOL (57011-48-0)

Safety Data

• Safety Statements: Mutation data reported. When heated to decomposition it emits toxic vapors of NOsub xmlns="">x/sub>.
• Hazardous Substances Data: 57011-48-0(Hazardous Substances Data)

Usage

Appearance

Colorless, crystalline solid

Stability

Highly explosive and sensitive to heat, shock, and friction

Uses

a. Production of energetic materials (explosives and propellants)
b. Cross-linking agent in polymer production
c. Reagent in organic synthesis

Safety precautions

Handle with extreme caution, only by trained professionals in a controlled laboratory environment.

Upstream product

• 96-23-1 1,3-Dichloro-2-propanol 
• 536-74-3 phenylacetylene 
• 106-89-8 epichlorohydrin 

Downstream Products

• 616-29-5 1,3-Diamino-2-hydroxypropane 
• 70017-51-5 1,3-Diazido-2-propyl-4,4,4-trinitrobutyrat 

Relevant articles and documents

Halohydrin dehalogenase-catalysed transformations of epifluorohydrin

Biocatalytic ring-opening of epifluorohydrin has been performed by using halohydrin dehalogenase. The enzyme from Mycobacterium sp. GP1 (HheB2) catalysed reaction with high regioselectivity and low enantioselectivity in the presence of different nucleophi

Zeo-click chemistry: Copper(I)-zeolite-catalyzed cascade reaction; One-pot epoxide ring-opening and cycloaddition

Copper(I)-modified zeolites, especially CuI-USY, proved to be very efficient catalysts in multi-component reactions of epoxides with sodium azide and terminal alkynes. Such catalysts allow highly regio- and stereoselective syntheses ofhydroxyme