16004-15-2 Usage
Description
4-Iodobenzyl bromide is an organic compound that exists as a light yellow adhering crystalline powder. It is characterized by its chemical structure, which includes a benzene ring with an iodine atom at the para position and a bromine atom attached to the benzyl group.
Uses
Used in Organic Synthesis:
4-Iodobenzyl bromide is used as an organic chemical synthesis intermediate for various applications in the chemical and pharmaceutical industries. Its unique structure allows it to be a versatile building block in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Iodobenzyl bromide is used as a key intermediate in the synthesis of various drugs and drug candidates. Its reactivity and functional groups make it suitable for the development of new therapeutic agents with potential applications in treating a wide range of diseases and medical conditions.
Used in Chemical Industry:
In the chemical industry, 4-Iodobenzyl bromide is utilized as an intermediate for the production of various specialty chemicals, such as dyes, pigments, and additives. Its unique properties enable it to be a valuable component in the formulation of these products, contributing to their performance and functionality.
Overall, 4-Iodobenzyl bromide is a versatile and valuable compound in the fields of organic synthesis, pharmaceuticals, and the chemical industry, serving as a crucial intermediate in the development of new and innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 16004-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,0 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16004-15:
(7*1)+(6*6)+(5*0)+(4*0)+(3*4)+(2*1)+(1*5)=62
62 % 10 = 2
So 16004-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6BrI/c8-5-6-1-3-7(9)4-2-6/h1-4H,5H2
16004-15-2Relevant articles and documents
Ethyl 2-formamido-2-(4-iodobenzyl)-3-(4-iodophenyl)propionate and ethyl 2-(3-bromobenzyl)-3-(3-bromophenyl)-2-formamidopropionate
Damodharan, Lakshminarasimhan,Pattabhi, Vasantha,Behera, Manoranjan,Kotha, Sambasivarao
, p. o216-o218 (2003)
The title compounds, C19H19I2NO3 and C19H19Br2NO3, are derivatives of α-aminoisobutyric acid with halogen substituents at the para and meta positions, respectively. The ethoxycarbonyl and formamide side chains attached to the Cαatom of the molecule adopt extended and folded conformations, respectively. The crystal structures are stabilized by N -H...O, C - H...O, C - Br...O and C - I...O interactions.
Carbonylative Coupling of Alkyl Zinc Reagents with Benzyl Bromides Catalyzed by a Nickel/NN2 Pincer Ligand Complex
Andersen, Thomas L.,Donslund, Aske S.,Neumann, Karoline T.,Skrydstrup, Troels
supporting information, p. 800 - 804 (2017/12/26)
An efficient catalytic protocol for the three-component assembly of benzyl bromides, carbon monoxide, and alkyl zinc reagents to give benzyl alkyl ketones is described, and represents the first nickel-catalyzed carbonylative coupling of two sp3-carbon fragments. The method, which relies on the application of nickel complexed with an NN2-type pincer ligand and a controlled release of CO gas from a solid precursor, works well with a range of benzylic bromides. Mechanistic studies suggest the intermediacy of carbon-centered radicals.
A General Strategy to Enhance the Performance of Dye-Sensitized Solar Cells by Incorporating a Light-Harvesting Dye with a Hydrophobic Polydiacetylene Electrolyte-Blocking Layer
Desta, Mekonnen Abebayehu,Liao, Chia-Wei,Sun, Shih-Sheng
, p. 690 - 697 (2017/03/22)
A unique strategy to suppress charge recombination effectively and enhance light harvesting in dye-sensitized solar cells (DSSCs) is demonstrated by the design of a new dipolar organic dye functionalized with a diacetylene unit, which is capable of underg
