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N-trifluoroacetyl-glycinyl-L-phenylalanine methyl ester is a complex organic compound with the chemical formula C12H12F3NO4. It is a derivative of phenylalanine, an essential amino acid, and is characterized by the presence of a trifluoroacetyl group and a glycinyl moiety. N-trifluoroacetyl-glycinyl-L-phenylalanine methyl ester is synthesized by combining glycine, phenylalanine, and a methyl ester group, with the trifluoroacetyl group providing additional stability and reactivity. It is often used in the synthesis of pharmaceuticals and other bioactive molecules due to its unique structure and properties. The compound's specific arrangement of atoms and functional groups allows it to participate in various chemical reactions, making it a valuable building block in organic chemistry and drug development.

4554-41-0

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4554-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4554-41-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,5 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4554-41:
(6*4)+(5*5)+(4*5)+(3*4)+(2*4)+(1*1)=90
90 % 10 = 0
So 4554-41-0 is a valid CAS Registry Number.

4554-41-0Downstream Products

4554-41-0Relevant academic research and scientific papers

The: Ortho -substituent on 2,4-bis(trifluoromethyl)phenylboronic acid catalyzed dehydrative condensation between carboxylic acids and amines

Wang, Ke,Lu, Yanhui,Ishihara, Kazuaki

, p. 5410 - 5413 (2018)

2,4-Bis(trifluoromethyl)phenylboronic acid is a highly effective catalyst for dehydrative amidation between carboxylic acids and amines. Mechanistic studies suggest that a 2:2 mixed anhydride is expected to be the only active species, and the ortho-substituent of boronic acid plays a key role in preventing the coordination of amines to the boron atom of the active species, thus accelerating the amidation. This catalyst works for α-dipeptide synthesis.

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