24449-05-6 Usage
Description
(4Z)-9,9-dibromobicyclo[6.1.0]non-4-ene, also known as 9,9-dibromobicyclo[6.1.0]nona-4,6-diene, is a bicyclic compound with a unique structure. It consists of a bicyclic nonane core with two bromine atoms attached to the double bond. This chemical is used in organic synthesis and as a building block for the preparation of various organic compounds. It has a range of potential applications in pharmaceuticals, agrochemicals, and materials science. Its distinct structure and reactivity make it a valuable intermediate for the synthesis of complex molecules. Additionally, its bromine substituents make it a useful precursor for further chemical transformations. Overall, (4Z)-9,9-dibromobicyclo[6.1.0]non-4-ene is a versatile compound with potential for various industrial and research applications.
Uses
Used in Pharmaceutical Industry:
(4Z)-9,9-dibromobicyclo[6.1.0]non-4-ene is used as a building block for the synthesis of various pharmaceutical compounds due to its unique structure and reactivity. It can be utilized in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
(4Z)-9,9-dibromobicyclo[6.1.0]non-4-ene is used as an intermediate in the synthesis of agrochemicals, such as pesticides and herbicides, due to its potential applications in this field.
Used in Materials Science:
(4Z)-9,9-dibromobicyclo[6.1.0]non-4-ene is used as a precursor for the development of new materials with specific properties, such as improved strength, durability, or chemical resistance, due to its distinct structure and bromine substituents.
Used in Organic Synthesis:
(4Z)-9,9-dibromobicyclo[6.1.0]non-4-ene is used as a versatile intermediate in organic synthesis for the preparation of a wide range of organic compounds, taking advantage of its unique structure and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 24449-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,4 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24449-05:
(7*2)+(6*4)+(5*4)+(4*4)+(3*9)+(2*0)+(1*5)=106
106 % 10 = 6
So 24449-05-6 is a valid CAS Registry Number.
24449-05-6Relevant articles and documents
Force-reactivity property of a single monomer is sufficient to predict the micromechanical behavior of its polymer
Akbulatov, Sergey,Tian, Yancong,Boulatov, Roman
supporting information; experimental part, p. 7620 - 7623 (2012/06/30)
We demonstrate an accurate prediction of the micromechanical behavior of a single chain of cyclopropanated polybutadiene, which is governed by rapid isomerization of the cyclopropane moieties at ~1.2 nN, from the force-rate correlation of this reaction measured in a small series of increasingly strained macrocycles. The data demonstrate that a single physical quantity, force, uniquely defines the dynamics across length scales from >100 to 1 nm and that strain imposed through molecular design and that imposed by micromanipulation techniques have equivalent effects on the kinetics of a chemical reaction. This represents a new method of screening potential monomers for applications in stress-responsive materials that could also facilitate atomistic interpretations of single-molecule force experiments.
trans-Cycloalkenes. Part 11. trans-Cyclonona-1,2,6-triene, a Transient Precursor of 2,3-Divinylcyclopentene
Connel, A. Christopher,Whitham, Gordon H.
, p. 989 - 994 (2007/10/02)
Three potential precursors of trans-cyclonona-1,2,6-triene (1), namely the allene-dioxolan (7), the allene-oxathiolan (14), and the dichlorocyclopropane (16) have been prepared starting ultimately from cyclo-octa-1,5-diene.Treatment of these precursors with BunLi under conditions appropriate to each case gave 2,3-divinylcyclopentene in moderate to good yields.It is considered that trans-cyclonona-1,2,6-triene is formed as transient intermediate.