732306-26-2 Usage
Uses
Used in Pharmaceutical Industry:
2-Bromo-5-(trifluoromethyl)phenylacetonitrile, 97% is used as a key intermediate for the synthesis of various pharmaceuticals, leveraging its reactivity to form diverse derivatives that contribute to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Bromo-5-(trifluoromethyl)phenylacetonitrile, 97% serves as an essential building block in the creation of novel agrochemicals, including pesticides and herbicides, due to its ability to participate in a range of chemical reactions to produce effective compounds.
Used in Organic Chemistry Research:
2-Bromo-5-(trifluoromethyl)phenylacetonitrile, 97% is utilized as a research chemical, providing scientists with a high-purity substance to explore its properties and reactivity in various chemical reactions, thereby advancing the understanding of organic chemistry and its applications.
Used in Chemical Development:
2-Bromo-5-(trifluoromethyl)phenylacetonitrile, 97% is employed in the development of new chemical processes and methodologies, taking advantage of its unique structural features and reactivity to innovate and improve upon existing synthetic routes.
Check Digit Verification of cas no
The CAS Registry Mumber 732306-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,2,3,0 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 732306-26:
(8*7)+(7*3)+(6*2)+(5*3)+(4*0)+(3*6)+(2*2)+(1*6)=132
132 % 10 = 2
So 732306-26-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H5BrF3N/c10-8-2-1-7(9(11,12)13)5-6(8)3-4-14/h1-2,5H,3H2
732306-26-2Relevant academic research and scientific papers
Construction of 2-Arylbenzo[4,5]thieno[2,3-d]thiazole Skeleton via CuCl/S-Mediated Three-Component Reaction
Zhang, Wei,Tao, Shanqing,Ge, Huaibin,Li, Qiao,Ai, Zhenkang,Li, Xiaoxian,Zhang, Beibei,Sun, Fengxia,Xu, Xiaqing,Du, Yunfei
supporting information, p. 448 - 452 (2020/02/04)
An exclusive thiophene-fused polycyclic I-conjugated 2-arylbenzo[4,5]thieno[2,3-d]thiazole skeleton was constructed via a one-pot CuCl-mediated three-component reaction, using 2-(2-bromophenyl)acetonitrile and aromatic aldehydes as substrates and elementa
Synthesis of benzylisoquinoline derivatives possessing electron-withdrawing substituents on the benzene ring of the isoquinoline skeleton
Severin, René,Mujahidin, Didin,Reimer, Jessica,Doye, Sven
, p. 683 - 700 (2008/09/18)
3,4-Dihydrobenzylisoquinolines and 1,2,3,4-tetrahydrobenzyl-isoquinolines possessing electron withdrawing substituents on the benzene ring of the isoquinoline framework are easily accessible by a synthetic approach that takes advantage of a Sonogashira coupling to build up the C1-C8a bond of the isoquinoline skeleton and a Ti-catalyzed intramolecular hydroamination of an alkyne to close the heterocyclic ring.
