7508-78-3 Usage
General Description
2-Chloro-N-(2-Methoxyphenyl)benzaMide, 97% is a chemical compound with the molecular formula C13H11ClN2O2. It is a white to off-white powder with a purity of 97%. 2-Chloro-N-(2-Methoxyphenyl)benzaMide, 97% is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used in the production of dyes, pigments, and other organic compounds. Additionally, it has been studied for its potential anti-cancer and anti-inflammatory properties. This chemical should be handled and stored in accordance with proper safety protocols and regulations.
Check Digit Verification of cas no
The CAS Registry Mumber 7508-78-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7508-78:
(6*7)+(5*5)+(4*0)+(3*8)+(2*7)+(1*8)=113
113 % 10 = 3
So 7508-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H12ClNO2/c1-18-13-9-5-4-8-12(13)16-14(17)10-6-2-3-7-11(10)15/h2-9H,1H3,(H,16,17)
7508-78-3Relevant articles and documents
Continuous flow photochemistry as an enabling synthetic technology: Synthesis of substituted-6(5: H)-phenanthridinones for use as poly(ADP-ribose) polymerase inhibitors
Fang,Tranmer
supporting information, p. 720 - 724 (2016/05/19)
Methods utilizing continuous flow photochemistry, an enabling synthetic technology, have been developed for the generation of phenanthridinones via an intramolecular photochemical cyclization of 2-chlorobenzamides for the purposes of generating poly(ADP-ribose) polymerase inhibitors. Herein we report 16 examples of a single-step flow photocyclization which produces substituted phenanthridinones in yields up to 99%, while a two-step method leads directly to phenanthridinones from 2-chlorobenzoyl chlorides and anilines via a novel continuous flow amidation/photocyclization protocol. Overall, the flow photocyclization reactions typically progress in good to excellent yields, and in a superior fashion to analogous batch methods, greatly enabling the drug discovery process.
