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2-(bis(trimethylsilyl)amino)phenyl bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54807-57-7

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54807-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54807-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,0 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54807-57:
(7*5)+(6*4)+(5*8)+(4*0)+(3*7)+(2*5)+(1*7)=137
137 % 10 = 7
So 54807-57-7 is a valid CAS Registry Number.

54807-57-7Relevant academic research and scientific papers

NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE INHIBITORS AND METHODS FOR USE OF THE SAME

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Paragraph 0087-0088; 0090, (2019/08/26)

Disclosed herein are compounds that can act as inhibitors of nicotinamide phosphoribosyltransferase ("NAMPT"), and methods for their use in treating or preventing diseases, such as pulmonary arterial hypertension ("PAH"). The compounds described herein ca

A synthetic amino acid frequency that alcohol ester

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Paragraph 0023; 0024; 0025, (2017/08/25)

The invention relates to a method of synthesizing aminophenylboronic acid pinacol ester. The method includes subjecting bromoaniline having different substitute positions to silanization protection, reacting with magnesium metal or butyl lithium, and performing boronization/deprotection/esterification to obtain a product. Raw materials and agents, which are adopted in the method, are cheap and easily available. Reaction conditions are mild. Only simple treatment is needed after a reaction in each step is finished. The method is capable of continuous operation. The total yield is 40-55%. The purity of the product is high. The method is suitable for large-scale amplification production.

Synthesis of N-and C-trimethylsilyl-substituded anililes

Storozhenko,Belyakova,Starikova,Nosova,Shulyat'eva,Frenkel',Pecherskii

, p. 892 - 897 (2008/12/20)

N-Metallation of bromoanilines with ethylmagnesium bromide followed by a reaction with trimethylchlorosilane provided N-mono and N-bis(trimethylsilyl) bromoanilines depending on the structure of substrate. The metallation of bissilylated bromoanilines with butyllithium permitted the introduction of a trimethylsilyl substituent in the aromatic ring. Previously unknown 2-bromo-N,N-bis(trimethylsilyl)aniline, 2,6-dibromo-N-trimethylsilylaniline, 2,6-dibromo-N,N-bis(trimethylsilyl)aniline, 2-bromo-6-trimethylsilylaniline, 2-bromo-6-trimethylsilyl-N,N-bis(trimethylsilyl)aniline, 2-bromo-6- trimethylsilyl-N-trimethylsilylaniline, 2,4,6-tribromo-N-trimethylsilylaniline, and 2,4,6-tribromo-N,N-bis(trimethylsilyl)aniline were prepared. The structures of the compounds obtained were established by the chromato-mass spectrometry and 1H, 13C, and 29Si NMR spectroscopy.

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