94201-83-9 Usage
Chemical structure
1,3-bis[2-(dimethylamino)phenyl]urea is a urea derivative with two dimethylamino phenyl groups attached to the central urea moiety.
Usage
Commonly used as a reagent in organic synthesis.
Catalytic activity
Potent catalyst for the transesterification of esters and the cross-coupling of aryl halides with arylboronic acids.
Application in pharmaceuticals
Used as a reactant in the preparation of various pharmaceuticals and agrochemicals.
Potential application in materials science
Studied for its potential application in materials science.
Luminescent properties
Investigated as a luminescent material in the development of organic light-emitting diodes (OLEDs).
Check Digit Verification of cas no
The CAS Registry Mumber 94201-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,0 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 94201-83:
(7*9)+(6*4)+(5*2)+(4*0)+(3*1)+(2*8)+(1*3)=119
119 % 10 = 9
So 94201-83-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H22N4O/c1-20(2)15-11-7-5-9-13(15)18-17(22)19-14-10-6-8-12-16(14)21(3)4/h5-12H,1-4H3,(H2,18,19,22)
94201-83-9Relevant academic research and scientific papers
Decomposition of 2-dialkylaminobenzoyl azides to yield isocyanates and 1,1 -dialky lindazol-1-ium-3-olates
Waldron, Norman M.,Raza, Muhammad
, p. 271 - 276 (2007/10/03)
Substituted benzoyl azides normally yield the correspondingly substituted isocyanates but when a dialkylated amino group is in the 2-position, in addition to the isocyanate, the 1,1-dialkylated indazol-1-ium-3-olate is produced. The ratio of the two products is very variable depending upon the substitution in the benzene ring. Largest yields of the zwitterionic products were found when there was a substituent in the 3-position regardless of whether the substituent was electron-donating or -withdrawing.
