172035-86-8 Usage
Description
3-Thienylmagnesium iodide is an organometallic compound that consists of a magnesium atom bonded to a 3-thienyl group and an iodide ion. It is recognized for its unique reactivity and selectivity, making it a valuable nucleophile in organic synthesis. 3-THIENYLMAGNESIUM IODIDE is adept at participating in various carbon-carbon and carbon-heteroatom bond-forming reactions, which is instrumental in the preparation of a diverse array of functional groups such as alcohols, amines, and ketones. Its synthesis typically involves the reaction of 3-bromothiophene with magnesium metal in the presence of iodine, followed by purification to isolate the desired product.
Uses
Used in Organic Synthesis:
3-Thienylmagnesium iodide is used as a nucleophilic reagent for facilitating a range of bond-forming reactions in organic synthesis. Its versatility lies in its ability to engage in the formation of carbon-carbon and carbon-heteroatom bonds, which is crucial for the synthesis of complex organic molecules.
Used in the Preparation of Functional Groups:
In the Pharmaceutical Industry, 3-thienylmagnesium iodide is utilized as a key intermediate for the synthesis of various functional groups, including alcohols, amines, and ketones. These functional groups are essential building blocks in the development of pharmaceutical compounds, contributing to the creation of new drugs with specific therapeutic properties.
Used in Academic and Industrial Research:
3-Thienylmagnesium iodide is employed as a research tool in both academic and industrial settings. Its unique reactivity and selectivity make it an attractive candidate for exploring new synthetic pathways and developing innovative methods in organic chemistry.
Used in the Synthesis of Thiophene-Containing Compounds:
In the Chemical Industry, 3-thienylmagnesium iodide is used as a precursor for the synthesis of thiophene-containing compounds, which are important in the production of various chemicals, materials, and pharmaceuticals. 3-THIENYLMAGNESIUM IODIDE's reactivity allows for the efficient construction of thiophene rings and their derivatives, which are valuable components in a wide range of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 172035-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,0,3 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 172035-86:
(8*1)+(7*7)+(6*2)+(5*0)+(4*3)+(3*5)+(2*8)+(1*6)=118
118 % 10 = 8
So 172035-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H3S.HI.Mg/c1-2-4-5-3-1;;/h1,3-4H;1H;/q-1;;+2/p-1
