1333240-71-3 Usage
Derivative of benzyl bromide
The compound is derived from benzyl bromide, which means it has a similar structure and properties.
Three iodine atoms attached
The benzene ring of the compound has three iodine atoms attached to it, which makes it highly reactive.
Reactivity
The presence of three iodine atoms makes the compound highly reactive and useful in a variety of chemical reactions.
Organic synthesis reagent
The compound is commonly used as a reagent in organic synthesis, particularly in the preparation of various pharmaceuticals and other organic compounds.
Introduction of iodine atoms
The compound is known for its ability to facilitate the introduction of iodine atoms into organic molecules, making it an important tool in the field of medicinal chemistry and drug discovery.
Production of radiolabeled compounds
The compound is also used in the production of radiolabeled compounds for medical imaging and diagnostic purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 1333240-71-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,2,4 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1333240-71:
(9*1)+(8*3)+(7*3)+(6*3)+(5*2)+(4*4)+(3*0)+(2*7)+(1*1)=113
113 % 10 = 3
So 1333240-71-3 is a valid CAS Registry Number.
1333240-71-3Relevant articles and documents
Synthesis and conjugation of a triiodohydroxylamine for the preparation of highly X-ray opaque poly(ε-caprolactone) materials
Van Horn, Brooke A.,Davis, Lundy L.,Nicolau, Samantha E.,Burry, Emma E.,Bailey, Victoria O.,Guerra, Fernanda D.,Alexis, Frank,Whitehead, Daniel C.
, p. 787 - 793 (2017)
To address a need for highly X-ray opaque biodegradable materials, a series of poly(ε-caprolactone) derivatives were prepared using oxime post-polymerization modification to conjugate two different iodinated hydroxylamines. These materials were synthesized with up to 32 wt. % iodine content and demonstrated improved X-ray contrast relative to both the ketone precursors and previously reported monoiodinated materials.
