405198-83-6 Usage
Description
(2-IODO-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER is a chemical compound characterized by the molecular formula C12H15IN2O2. It is synthesized through the reaction between (2-iodo-benzyl)amine and tert-butyl chloroformate. (2-IODO-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER plays a significant role in the field of organic chemistry and chemical synthesis due to its versatile applications.
Uses
Used in Pharmaceutical Industry:
(2-IODO-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER is utilized as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs and medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, (2-IODO-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER serves as an intermediate for the production of agrochemicals. Its involvement in the synthesis process contributes to the development of effective pesticides and other agricultural chemicals.
Used in Dye and Pigment Production:
(2-IODO-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER is also employed as an intermediate in the manufacturing of certain dyes and pigments. Its chemical properties allow for the creation of a wide range of colorants used in various industries, including textiles, plastics, and printing.
Check Digit Verification of cas no
The CAS Registry Mumber 405198-83-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,5,1,9 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 405198-83:
(8*4)+(7*0)+(6*5)+(5*1)+(4*9)+(3*8)+(2*8)+(1*3)=146
146 % 10 = 6
So 405198-83-6 is a valid CAS Registry Number.
405198-83-6Relevant articles and documents
Super-Electron-Donor 2-Azaallyl Anions Enable Construction of Isoquinolines
Chen, Wen,Cong, Jielun,Deng, Guogang,Duan, Shengzu,Jing, Hong,Li, Minyan,Walsh, Patrick J.,Yang, Xiaodong,Yin, Meng,Zi, Quanxing
, p. 1786 - 1790 (2022/03/14)
Herein is introduced the application of “super-electron-donor”(SED) 2-azaallyl anions in a tandem reduction/radical cyclization/radical coupling/aromatization protocol that enables the rapid construction of isoquinolines. The value of this transition-metal-free method is highlighted by the wide range of isoquinoline ethyl amines prepared with good functional group tolerance and yields. An operationally simple gram scale synthesis is also conducted, confirming the scalability.
Cyclization reactions of 2-alkynylbenzyl alcohol and 2-alkynylbenzylamine derivatives promoted by tetrabutylammonium fluoride
Hiroya, Kou,Jouka, Rumi,Kameda, Mitsuyoshi,Yasuhara, Akito,Sakamoto, Takao
, p. 9697 - 9710 (2007/10/03)
The regioselectivity of the cyclization reaction of 2-ethynylbenzyl alcohol and 2-ethynylbenzylamine derivatives promoted by TBAF was investigated. Six-membered ring derivatives were obtained from the compounds, which have a butyl group on the triple bond. Whereas five-membered ring products were afforded from the substrates having hydrogen or aromatic substituents on the acetylene moiety. It was also concluded that both the tetrabutylammonium cation and fluoride anion were essential for the cyclization. Thus, the actual mechanism and catalytic cycle were also suggested.
