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L-Leucine, N-(phenylmethylene)-, ethyl ester is a chemical compound that belongs to the class of ethyl esters and is derived from the amino acid L-leucine. It is commonly used in the field of organic chemistry and biochemistry as a building block for synthesizing various compounds.

2743-41-1

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2743-41-1 Usage

Uses

Used in Pharmaceutical Industry:
L-Leucine, N-(phenylmethylene)-, ethyl ester is used as a building block for the development of new drugs and medications, contributing to the advancement of pharmaceutical formulations and therapies.
Used in Nutrition and Athletic Supplements:
L-Leucine, N-(phenylmethylene)-, ethyl ester is used as a nutritional supplement to support protein synthesis and metabolism, particularly for athletes and individuals seeking to improve muscle growth and recovery.
Used in Research and Laboratory Settings:
L-Leucine, N-(phenylmethylene)-, ethyl ester is used as a research compound for studying protein synthesis and metabolism, aiding in the understanding of biological processes and the development of new therapeutic approaches.

Check Digit Verification of cas no

The CAS Registry Mumber 2743-41-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,4 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2743-41:
(6*2)+(5*7)+(4*4)+(3*3)+(2*4)+(1*1)=81
81 % 10 = 1
So 2743-41-1 is a valid CAS Registry Number.

2743-41-1Relevant academic research and scientific papers

Boron Trifluoride Assisted Perfluoroalkylation of Carbon-Nitrogen Double Bonds

Uno, Hidemitsu,Okada, Shin-ichiro,Ono, Tetsushi,Shiraishi, Yasukazu,Suzuki, Hitomi

, p. 1504 - 1513 (2007/10/02)

In the presence of BF3*OEt2, (perfluoroalkyl)lithiums generated in situ from the reaction of primary perfluoroalkyl iodides and MeLi-LiBr reacted with imines, azines, and nitrones to afford perfluoroalkylated nitrogen-containing compounds in moderate to good yields.This method was successfully applied to the preparation of a (perfluoroalkyl)glycine and optically active perfluoroalkylated amines.

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