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methyl N-(2-bromo-4-methylphenyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

540797-44-2

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540797-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 540797-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,0,7,9 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 540797-44:
(8*5)+(7*4)+(6*0)+(5*7)+(4*9)+(3*7)+(2*4)+(1*4)=172
172 % 10 = 2
So 540797-44-2 is a valid CAS Registry Number.

540797-44-2Relevant academic research and scientific papers

Chiral Bifunctional Phosphine-Carboxylate Ligands for Palladium(0)-Catalyzed Enantioselective C?H Arylation

Yang, Lei,Neuburger, Markus,Baudoin, Olivier

supporting information, p. 1394 - 1398 (2018/01/05)

Previous enantioselective Pd0-catalyzed C?H activation reactions proceeding via the concerted metalation-deprotonation mechanism employed either a chiral ancillary ligand, a chiral base, or a bimolecular mixture thereof. This study describes th

Palladium-Catalyzed Carbamate-Directed Regioselective Halogenation: A Route to Halogenated Anilines

Moghaddam, Firouz Matloubi,Tavakoli, Ghazal,Saeednia, Borna,Langer, Peter,Jafari, Behzad

, p. 3868 - 3876 (2016/05/24)

This study describes an efficient method for ortho-selective halogenation of N-arylcarbamates under mild conditions for the first time. Although being weakly coordinating, N-arylcarbamates act very well as a removable directing group for activation of C-H bonds. The developed procedure results in extremely valuable halogenated N-arylcarbmates that can further be hydrolyzed to halogenated anilines. The obtained reaction conditions showed broad scope and wide functional group tolerance. All the products were formed in good yields with extremely high selectivity.

Synthesis of 5,6-dihydrophenanthridines via N,O-acetal TMS ethers

Lee, Won-Il,Jung, Jong-Wha,Jang, Jaebong,Yun, Hwayoung,Suh, Young-Ger

, p. 5167 - 5171 (2013/09/02)

A concise and high-yielding protocol for the synthesis of 5,6-dihydrophenanthridines is disclosed. The key feature includes a sequential reduction-cyclization reaction of N-acylcarbamates via N,O-acetal TMS ethers as a stable N-acyliminium ion precursor.

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