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1,1-dimethyl-3-[4-(trifluoromethyl)phenyl]urea is an organic compound with the molecular formula C10H10F3N2O. It is a white crystalline solid that belongs to the class of urea derivatives, characterized by the presence of a urea functional group (-NH-CO-NH-). The molecule features a trifluoromethyl group (-CF3) attached to a phenyl ring, which is in turn connected to the urea moiety through a methylene bridge. This chemical is primarily used as an intermediate in the synthesis of various agrochemicals, pharmaceuticals, and other specialty chemicals. Due to its unique structure and properties, it has potential applications in the development of new compounds with specific biological activities.

7159-99-1

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7159-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7159-99-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7159-99:
(6*7)+(5*1)+(4*5)+(3*9)+(2*9)+(1*9)=121
121 % 10 = 1
So 7159-99-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-7(4-6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)

7159-99-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name parafluron

1.2 Other means of identification

Product number -
Other names Caswell No. 387

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7159-99-1 SDS

7159-99-1Downstream Products

7159-99-1Relevant academic research and scientific papers

Cu(II)-Catalyzed Ortho-C-H Nitration of Aryl Ureas by C-H Functionalization

Wang, Chun-Meng,Tang, Kai-Xiang,Gao, Tian-Hong,Chen, Lin,Sun, Li-Ping

, p. 8315 - 8321 (2018/07/15)

A novel protocol for the aromatic ortho C-H nitration of aryl ureas with Fe(NO3)3·9H2O is developed. The reaction utilizes CuCl2·2H2O as catalyst and p-TSA as additive, showing good functional group tolerance and furnishing the desired products in moderate to excellent yields.

Transition Metal-Free Carbazole Synthesis from Arylureas and Cyclohexanones

Wu, Jun,Xie, Yanjun,Chen, Xiangui,Deng, Guo-Jun

supporting information, p. 3206 - 3211 (2016/10/21)

An efficient strategy for carbazole synthesis from arylureas and cyclohexanones under transition metal-free conditions has been developed. The combined use of potassium iodide and iodine could significantly improve the reaction efficiency to provide 2,6-disubstituted 9-arylcarbazoles in moderate to good yields. In this kind of transformation, the whole carbazole moiety (except the nitrogen atom) comes from two equivalents of cyclohexanones. (Figure presented.).

Comparative catalytic C-H vs. C-Si activation of arenes with Pd complexes directed by urea or amide groups

Rauf, Waqar,Thompson, Amber L.,Brown, John M.

supporting information; experimental part, p. 3874 - 3876 (2010/01/06)

Analysis of regiocontrol in Pd-catalysed C-H activation leads to observations of aryltrimethylsilyl activation and to superior results with urea-based substrates.

Distinct reactivity of Pd(OTs)2: The intermolecular Pd(II)-catalyzed 1,2-carboamination of dienes

Houlden, Chris E.,Bailey, Chris D.,Ford, J. Gair,Gagne, Michel R.,Lloyd-Jones, Guy C.,Booker-Milburn, Kevin I.

supporting information; experimental part, p. 10066 - 10067 (2009/02/04)

A Pd-catalyzed intermolecular 1,2-carboamination route to indolines from N-aryl ureas and 1,3-dienes that proceeds under mild conditions in relatively nonacidic media, is presented. The in situ generation, or preformation, of a palladium tosylate emerges as a key parameter in gaining the requisite reactivity for the C-H insertion/carbopalladation/nucleophilic displacement process. Copyright

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