15965-30-7 Usage
Description
4,5-Dichloroimidazole is an organic compound with the molecular formula C3H3Cl2N2. It is characterized by the presence of two chlorine atoms at the 4,5-positions of the imidazole ring. 4,5-Dichloroimidazole is known for its versatile chemical properties and potential applications in various fields.
Uses
Used in Chemical Synthesis:
4,5-Dichloroimidazole is used as a key intermediate in the synthesis of various chemical compounds, such as phosphinite complexes and 1-hexyl-3-methyl-4,5-dichloroimidazolium iodide. Its unique structure and reactivity make it a valuable building block for creating new molecules with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,5-Dichloroimidazole is used as a precursor for the preparation of silver-carbene complex-loaded L-tyrosine polyphosphate nanoparticles. These nanoparticles have potential applications in drug delivery systems, offering improved targeting and release of therapeutic agents.
Used in Material Science:
4,5-Dichloroimidazole's chemical properties also make it a candidate for use in the development of new materials with specific characteristics, such as improved stability, reactivity, or selectivity. Its potential applications in material science could lead to the creation of novel materials for various industries, including electronics, energy, and environmental protection.
Check Digit Verification of cas no
The CAS Registry Mumber 15965-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,6 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15965-30:
(7*1)+(6*5)+(5*9)+(4*6)+(3*5)+(2*3)+(1*0)=127
127 % 10 = 7
So 15965-30-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H2Cl2N2/c4-2-3(5)7-1-6-2/h1H,(H,6,7)
15965-30-7Relevant articles and documents
Fast halogenation of some N-heterocycles by means of N,N'-dihalo-5,5- dimethylhydantoin
Sandtorv, Alexander H.,Bjorsvik, Hans-Rene
, p. 499 - 507 (2013/05/08)
An instantaneous, selective and high-yielding halogenation process is reported. The method operates with imidazoles, pyrazoles, and indoles under benign reaction conditions. The developed process involves the use of N,N'-dihalo-5,5-dimethylhydantoins (halo=chlorine, bromine, iodine) as halogenation reagents that are activated by catalytic quantities of a strong Bronsted acid. Moreover, the halogenation process is switchable to produce either the mono- or di-halogenated products. Issues related to the reaction mechanism are investigated and a proposal for a reaction mechanism is disclosed.
Katalytische Synthesen funktionalisierter Stickstoffheterocyclen aus Dicyan
Sundermeyer, Joerg,Roesky, Herbert W.
, p. 1417 - 1418 (2007/10/02)
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