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N-[3-(benzoylamino)phenyl]-5-bromonaphthalene-1-carboxamide is a complex organic compound with the molecular formula C23H16BrN2O2. It is characterized by a naphthalene-1-carboxamide core, which is substituted with a bromo group at the 5-position. The naphthalene ring is further connected to a benzoylamino group at the 3-position of the phenyl ring. N-[3-(benzoylamino)phenyl]-5-bromonaphthalene-1-carboxamide is a member of the carboxamide class and is known for its potential applications in the field of pharmaceuticals and materials science, particularly as a building block for the synthesis of more complex molecules or as a chemical intermediate. Its specific properties and uses can vary widely depending on the context in which it is applied, and further research may be required to fully understand its potential applications and effects.

5840-78-8

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5840-78-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5840-78-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5840-78:
(6*5)+(5*8)+(4*4)+(3*0)+(2*7)+(1*8)=108
108 % 10 = 8
So 5840-78-8 is a valid CAS Registry Number.

5840-78-8Relevant academic research and scientific papers

Development of a rapid, room-temperature dynamic kinetic resolution for efficient asymmetric synthesis of α-aryl amino acids

Hang, Jianfeng,Li, Hongming,Deng, Li

, p. 3321 - 3324 (2007/10/03)

equation presented A rapid, highly efficient and general dynamic kinetic resolution (DKR) of racemic α-aryl UNCAs with the dual-function catalysis of modified cinchona alkaloid was accomplished at room temperature. This DKR led to the development of a highly enantioselective catalytic method for the practical synthesis of a wide range of α-aryl and α-heteroaryl amino acids in 89-92% ee and 86-95% yield from racemic UNCAs.

ENANTIOMERIC QUANTIFICATIONS OF AMINO ACIDS THROUGH THEIR Nα-ACYL AMIDES BY GAS CHROMATOGRAPHY.

Hosten, N.,Anteunis, M. J. O.

, p. 45 - 47 (2007/10/02)

Apparent separation of 1.1 or higher on Chiralsil Val III can be obtained for Nα-acyl N-alkyl aminoacid amides allowing the use of short capillary gas chromatographic columns.A clean derivatization protocol without racemization is described, proceding through the NCA derivatives that are prepared from "in situ" silylated amino acids with trimethylsilyl cyanide.

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