386267-31-8 Usage
Description
Ethyl 3-bromo-4-iodobenzoate is a chemical compound that belongs to the class of esters. It is a versatile building block in organic chemistry, known for its ability to react with a variety of reagents to form new compounds. Ethyl 3-bromo-4-iodobenzoate is primarily used in organic synthesis and pharmaceutical research, and is often utilized as an intermediate in the production of various pharmaceuticals and agrochemicals. Ethyl 3-bromo-4-iodobenzoate has also been studied for its potential anti-inflammatory and analgesic properties, making it a compound of interest in drug discovery and development.
Uses
Used in Pharmaceutical Research:
Ethyl 3-bromo-4-iodobenzoate is used as an intermediate in the production of various pharmaceuticals. Its versatility in reacting with different reagents makes it a valuable building block in the synthesis of new compounds for drug development.
Used in Agrochemical Production:
Ethyl 3-bromo-4-iodobenzoate is also utilized as an intermediate in the production of agrochemicals, contributing to the development of new compounds for agricultural applications.
Used in Drug Discovery and Development:
Due to its potential anti-inflammatory and analgesic properties, Ethyl 3-bromo-4-iodobenzoate is a compound of interest in drug discovery and development. Researchers are exploring its potential applications in the creation of new medications for various therapeutic areas.
It is important to handle Ethyl 3-bromo-4-iodobenzoate with proper care and adhere to safety guidelines, as it may pose potential health and environmental hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 386267-31-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,6,2,6 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 386267-31:
(8*3)+(7*8)+(6*6)+(5*2)+(4*6)+(3*7)+(2*3)+(1*1)=178
178 % 10 = 8
So 386267-31-8 is a valid CAS Registry Number.
386267-31-8Relevant articles and documents
Flexible, Linear Chains Act as Baffles To Inhibit the Intramolecular Rotation of Molecular Turnstiles
Yu, Chengyuan,Ma, Lishuang,He, Jiaojiao,Xiang, Junfeng,Deng, Xuebin,Wang, Ying,Chen, Xuebo,Jiang, Hua
, p. 15849 - 15852 (2016)
In artificial molecular devices, flexible, linear chains typically exhibit very weak capability in inhibiting molecular motion. Herein, we describe the dynamic properties of a series of molecular turnstiles consisting of a rigid frame and a phenyl rotator flanked with linear alkoxymethyl substituents. The long, flexible substituents act as elastic baffles to inhibit the rotations of the rotator at medium to fast speeds on the NMR time scale. When the rotator moves slowly, the substituents become more relaxed, thus obtaining an opportunity to completely thread through the cavity of the turnstiles. These findings reveal a basic but missing correlation between steric hindrance and speed of motion for flexible, linear chains in dynamic molecular devices, thus opening up a new direction toward molecular machines with more elaborate dynamic functions.
Synthesis of pyrene containing building blocks for dendrimer synthesis
Modrakowski,Flores,Beinhoff,Schlueter
, p. 2143 - 2155 (2007/10/03)
Efficient syntheses of the novel, pyrene containing branched building blocks 10, 13, 22, 25 and of a pyrene based core molecule 16 for the construction of dendrimers are reported. The main tool is a Suzuki cross-coupling. The functional groups for further growth are amines and carboxylic acids, which were used in an orthogonally protected fashion. It was proven that the building blocks could be assembled to a low generation dendrimer 17.