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Urea, N'-(4-methylphenyl)-N-phenyl-N-(phenylmethyl)-, also known as 1-(4-methylphenyl)-3-phenyl-3-(phenylmethyl)urea, is an organic compound with the molecular formula C20H20N2O. It is a white crystalline solid that is soluble in organic solvents. Urea, N'-(4-methylphenyl)-N-phenyl-N-(phenylmethyl)- is a derivative of urea, where the two hydrogen atoms of the urea molecule are replaced by a 4-methylphenyl group, a phenyl group, and a phenylmethyl group. It is used in various applications, including as a chemical intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as in the production of dyes and pigments. Due to its complex structure, it is important to handle this chemical with care, following proper safety protocols to minimize potential health and environmental risks.

35113-69-0

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35113-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35113-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,1 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35113-69:
(7*3)+(6*5)+(5*1)+(4*1)+(3*3)+(2*6)+(1*9)=90
90 % 10 = 0
So 35113-69-0 is a valid CAS Registry Number.

35113-69-0Relevant academic research and scientific papers

DIAZANICKELACYCLOPENTANONE AUS NICKEL(0), IMINEN UND ISOCYANATEN

Hoberg, Heinz,Suemmermann, Klaus

, p. 383 - 390 (1983)

Isocyanates are oxidatively coupled with imines at nickel(0) under the influence of basic chelate ligands to form diazanickelacyclopentanones.The structure of these novel five-membered nickelacycles has been determined by spectroscopic and chemical methods.The mechanism of the coupling reaction is discussed.

Substituted diarylmethylamines by stereospecific intramolecular electrophilic arylation of lithiated ureas

Clayden, Jonathan,Dufour, Jeremy,Grainger, Damian M.,Helliwell, Madeleine

, p. 7488 - 7489 (2008/02/11)

On lithiation, N-benzyl ureas varying N′-aryl substituents undergo a migration of the aryl ring to the ∞ carbon of the N-benzyl group. With chiral, enantiomerically pure N-∞-methylbenzyl ureas, the rearrangement is stereospecific and creates a new, fully substituted stereogenic center ∞ to N. Removal of the urea function by N-nitrosation and hydrolysis allows the synthesis of chiral tertiary carbinamines in high enantiomeric purity. Copyright

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