200711-18-8 Usage
Appearance
Pale yellow solid The compound has a pale yellow color and is a solid at room temperature.
Usage
Intermediate in pharmaceuticals and agrochemicals It is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals.
Functional groups
Nitro and trifluoromethyl The presence of these functional groups makes the compound valuable in organic chemistry.
Additional applications
Dyes, pigments, and specialty chemicals The compound is also used in the production of dyes, pigments, and other specialty chemicals.
Stability
Relatively stable and non-reactive under normal conditions The compound is considered to be stable and non-reactive, but it should still be handled with caution.
Potential hazards
Handling precautions Due to its potential hazards, it is important to handle 2-(2-nitro-5-(trifluoromethyl)phenyl)acetonitrile with care.
Check Digit Verification of cas no
The CAS Registry Mumber 200711-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,7,1 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 200711-18:
(8*2)+(7*0)+(6*0)+(5*7)+(4*1)+(3*1)+(2*1)+(1*8)=68
68 % 10 = 8
So 200711-18-8 is a valid CAS Registry Number.
200711-18-8Relevant articles and documents
Active and Recyclable Catalytic Synthesis of Indoles by Reductive Cyclization of 2-(2-Nitroaryl)acetonitriles in the Presence of Co-Rh Heterobimetallic Nanoparticles with Atmospheric Hydrogen under Mild Conditions
Choi, Isaac,Chung, Hyunho,Park, Jang Won,Chung, Young Keun
supporting information, p. 5508 - 5511 (2016/11/17)
A cobalt-rhodium heterobimetallic nanoparticle-catalyzed reductive cyclization of 2-(2-nitroaryl)acetonitriles to indoles has been achieved. The tandem reaction proceeds without any additives under the mild conditions (1 atm H2 and 25 °C). This procedure could be scaled up to the gram scale. The catalytic system is significantly stable under these reaction conditions and could be reused more than ten times without loss of catalytic activity.
