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Benzamide, 2-bromo-4-methoxy-N,N-bis(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

666747-07-5

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666747-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 666747-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,6,7,4 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 666747-07:
(8*6)+(7*6)+(6*6)+(5*7)+(4*4)+(3*7)+(2*0)+(1*7)=205
205 % 10 = 5
So 666747-07-5 is a valid CAS Registry Number.

666747-07-5Downstream Products

666747-07-5Relevant academic research and scientific papers

Identification of key functionalization species in the Cp?Ir(iii)-catalyzed-: ortho halogenation of benzamides

Brown, Caleb A.,Guzmán Santiago, Alexis J.,Ison, Elon A.,Sommer, Roger D.

, p. 16166 - 16174 (2020/12/03)

Cp?Ir(iii) complexes have been shown to be effective for the halogenation of N,N-diisopropylbenzamides with N-halosuccinimide as a suitable halogen source. The optimized conditions for the iodination reaction consist of 0.5 mol% [Cp?IrCl2]2 in 1,2-dichlor

Nickel or phenanthroline mediated intramolecular arylation of sp 3 C-H bonds using aryl halides

Wertjes, William C.,Wolfe, Lydia C.,Waller, Peter J.,Kalyani, Dipannita

, p. 5986 - 5989 (2014/01/06)

The development of the intramolecular arylation of sp3 C-H bonds adjacent to nitrogen using aryl halides is described. Arylation was accomplished using either Ni(COD)2 or 1,10-phenanthroline in substoichiometric amounts, and the reaction conditions were applied to a variety of electronically differentiated benzamide substrates. Preliminary studies suggest a mechanism involving aryl and alkyl radical intermediates.

High-yielding, versatile, and practical [Rh(III)Cp*]-catalyzed ortho bromination and iodination of arenes

Schroeder, Nils,Wencel-Delord, Joanna,Glorius, Frank

, p. 8298 - 8301 (2012/06/29)

We report a uniquely high-yielding, general, and practical ortho bromination and iodination reaction of different classes of aromatic compounds. This reaction occurs by Rh(III)-catalyzed C-H bond activation methodology and is therefore the first example of the application of this cationic catalyst for C-Br and C-I bond formation.

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