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1,1-diisopropyl-3-methyl-3-phenylurea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82504-15-2

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82504-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82504-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,5,0 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82504-15:
(7*8)+(6*2)+(5*5)+(4*0)+(3*4)+(2*1)+(1*5)=112
112 % 10 = 2
So 82504-15-2 is a valid CAS Registry Number.

82504-15-2Downstream Products

82504-15-2Relevant academic research and scientific papers

A facile method for the preparation of unsymmetrical ureas utilizing zirconium (IV) chloride

Lee, Anna,Kim, Hee-Kwon,Thompson, David H.

, p. 154 - 160 (2016/02/26)

A facile synthetic method for the preparation of unsymmetrical ureas from amines is described. Carbamoyl imidazole compounds were prepared by the reaction of 1, 1-carbonyldiimidazole with primary or secondary amines, and further activation by treatment with zirconium(IV) chloride to generate the desired urea. This reaction protocol was applied to the synthesis of tri and tetrasubstituted ureas with high yields. This study provides an alternative guideline for the practical preparation of various unsymmetrical ureas.

Hindered ureas as masked isocyanates: Facile carbamoylation of nucleophiles under neutral conditions

Hutchby, Marc,Houlden, Chris E.,Gair Ford,Tyler, Simon N. G.,Gagne, Michel R.,Lloyd-Jones, Guy C.,Booker-Milburn, Kevin I.

supporting information; experimental part, p. 8721 - 8724 (2010/01/16)

Bigger is better: Sterically hindered dialkyl ureas undergo nucleophilic substitution at dramatically faster rates than their less hindered counterparts (see scheme). Steric decompression upon the formation of an intermediate isocyanate can explain this c

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