17200-53-2 Usage
Description
2-(Bromomethyl)acrylonitrile, also known as 2-Cyanoallyl Bromide, is an organic compound characterized by its unique structure that features a bromomethyl group and an acrylonitrile moiety. This molecule is known for its reactivity and potential applications in various industries due to its versatile chemical properties.
Uses
Used in Polymer Industry:
2-(Bromomethyl)acrylonitrile is used as a monomer for the synthesis of radically photopolymerizable compositions. Its application is particularly valuable because it contributes to the development of materials with high sensitivity and storage stability, which are crucial for various industrial applications, including coatings, adhesives, and printing inks.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 2-(Bromomethyl)acrylonitrile, due to its reactive nature, could potentially be used as an intermediate in the synthesis of pharmaceutical compounds. Its ability to form covalent bonds with other molecules makes it a candidate for the development of new drugs or drug delivery systems.
Used in Chemical Synthesis:
2-(Bromomethyl)acrylonitrile can also be utilized as a building block in the synthesis of various organic compounds, such as dyes, agrochemicals, and other specialty chemicals. Its reactivity allows for the creation of a wide range of products with different applications across multiple industries.
Check Digit Verification of cas no
The CAS Registry Mumber 17200-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,0 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17200-53:
(7*1)+(6*7)+(5*2)+(4*0)+(3*0)+(2*5)+(1*3)=72
72 % 10 = 2
So 17200-53-2 is a valid CAS Registry Number.
17200-53-2Relevant articles and documents
Chain extension of aldonolactones by samarium iodide mediated Dreiding- Schmidt reactions and samarium assisted Imamoto reactions
Csuk, Rene,Hoering, Ulrike,Schaade, Martina
, p. 9759 - 9776 (1996)
Unprecedented SmI2 mediated Dreiding-Schmidt reactions were used for chain extension reactions of aldonolactones with alkyl 2-bromomethyl acrylates or 2-bromomethyl-acrylonitrile, respectively. The reaction of aldonolactones with diiodomethane
Copper-Catalyzed Intermolecular Alkynylation and Allylation of Unactivated C(sp3)-H Bonds via Hydrogen Atom Transfer
Liang, Lei,Guo, Ge,Li, Chen,Wang, Song-Lin,Wang, Yue-Hui,Guo, Hai-Ming,Niu, Hong-Ying
supporting information, p. 8575 - 8579 (2021/11/13)
We describe Cu-catalyzed intermolecular alkynylation and allylation of unactivated C(sp3)-H bonds with singly occupied molecular orbital-philes (SOMO-philes) via hydrogen atom transfer (HAT). Employing N-fluoro-sulfonamide as a HAT reagent, a set of subst
Intermolecular Aminoallylation of Alkenes Using Allyl-Oxyphthalimide Derivatives: A Case Study in Radical Polarity Effects
Lardy, Samuel W.,Schmidt, Valerie A.
supporting information, p. 6796 - 6799 (2019/11/03)
A case study on the polarity effects of radical mediated intermolecular alkene aminoallylation is presented herein. This radical group transfer method pairs vinyl ethers with electronically deficient allyl-oxyphthalimide derivatives to give difunctionalized products while illustrating the guiding effects of polarity on this radical reactivity.
