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105908-83-6

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105908-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105908-83-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,0 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105908-83:
(8*1)+(7*0)+(6*5)+(5*9)+(4*0)+(3*8)+(2*8)+(1*3)=126
126 % 10 = 6
So 105908-83-6 is a valid CAS Registry Number.

105908-83-6Downstream Products

105908-83-6Relevant academic research and scientific papers

Efficient Direct Halogenation of Unsymmetrical N -Benzyl- and N -Phenylureas with Trihaloisocyanuric Acids

Sanabria, Carlos M.,Costa, Bruno B. S.,Viana, Gil M.,De Aguiar, Lúcia C. S.,De Mattos, Marcio C. S.

, p. 1359 - 1367 (2017/12/26)

A simple and efficient methodology for the direct halogenation of N -phenylureas was developed using trihaloisocyanuric acids in acetonitrile at room temperature. This protocol proved to be effective for the construction of N -phenylureas with different patterns of substitution. Additionally, less reactive N -benzylureas were halogenated in the presence of a mixture of trifluoroacetic acid and acetonitrile at room temperature.

Synthesis of some N-alkyl substituted urea derivatives as antibacterial and antifungal agents

Zheng, Qing-Zhong,Cheng, Kui,Zhang, Xiao-Min,Liu, Kai,Jiao, Qing-Cai,Zhu, Hai-Liang

experimental part, p. 3207 - 3212 (2010/08/20)

A series of N-alkyl substituted urea derivatives were synthesized and evaluated for their in vitro antibacterial and antifungal activities. The N-alkyl substituted urea derivatives bearing morpholine moiety (3a-3k) showed better activities than those bearing diethylamine moiety (2a-2f). Compounds having fluoro substituent at ortho (3c) and para (3b) positions of the phenyl ring exhibited potent antimicrobial activities against Gram-positive and Gram-negative bacteria as well as fungi.

Carbonyldiimidazole-mediated lossen rearrangement

Dube, Pascal,Fine Nathel, Noah F.,Vetelino, Michael,Couturier, Michel,Aboussafy, Claude Larrivee,Pichette, Simon,Jorgensen, Matthew L.,Hardink, Mark

supporting information; experimental part, p. 5622 - 5625 (2010/03/02)

[Chemical Equation Presented] Carbonyldiimidazole (CDI) was found to mediate the Lossen rearrangement of various hydroxamic acids to isocyanates. This process is experimentally simple and mild, with imidazole and CO 2 being the sole stoichiometric byproduct. Significant for large-scale application, the method avoids the use of hazardous reagents and thus represents a green alternative to standard processing conditions for the Curtius and Hofmann rearrangements.

Thiol on silica as a 'catch and release' support for isocyanates to afford ureas

Bolshan, Yuri,Tomaszewski, Miroslaw J.,Santhakumar, Vijayaratnam

, p. 4925 - 4927 (2008/02/08)

Silica-bound thiocarbamates were prepared by Curtius rearrangement of carboxylic acids in the presence of thiol on silica gel. The solid supported thiocarbamates were found to be stable isocyanate equivalents, which upon treatment with amines efficiently afforded di- and tri-substituted ureas. The urea products released from the catch and release support were, in the majority of cases, greater than 95% pure and required no further work up.

A novel synthesis of isocyanates and ureas via β-elimination of haloform

Braverman,Cherkinsky,Kedrova,Reiselman

, p. 3235 - 3238 (2007/10/03)

A novel synthesis of isocyanates via base-induced β-elimination of haloform from N-monosubstituted trihaloacetamides is described. The rate of reaction exhibits a strong dependence on the nature of the trihalomethyl group. Thus, while the reaction of tribromoacetamides proceeds at room temperature and the reaction of trichloroacetamides requires heating in polar solvents, no reaction could be observed for any of the corresponding trifluoro derivatives. This novel β-elimination of haloform from stable and readily available trihaloacetamides was applied to a 'one-pot' synthesis of ureas which avoids the use of phosgene and isolation of isocyanates.

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