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N-(Trifluoroacetyl)-L-leucine butyl ester is a synthetic chemical compound with the molecular formula C12H18F3NO3. It is a derivative of L-leucine, an essential amino acid, and is characterized by the presence of a trifluoroacetyl group and a butyl ester group. N-(Trifluoroacetyl)-L-leucine butyl ester is primarily used as a reagent in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. Its unique structure, which includes the trifluoromethyl group, imparts specific properties that can enhance the activity or stability of the final product. The compound is typically synthesized through a series of chemical reactions involving L-leucine and other reagents, and its use in research and industry highlights the importance of understanding and manipulating the properties of amino acid derivatives.

2796-38-5

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2796-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2796-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,9 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2796-38:
(6*2)+(5*7)+(4*9)+(3*6)+(2*3)+(1*8)=115
115 % 10 = 5
So 2796-38-5 is a valid CAS Registry Number.

2796-38-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Trifluoracetyl-leucin-n-butylester

1.2 Other means of identification

Product number -
Other names N-(Trifluoroacetyl)-L-leucine butyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2796-38-5 SDS

2796-38-5Downstream Products

2796-38-5Relevant academic research and scientific papers

Are Highly Stable Covalent Organic Frameworks the Key to Universal Chiral Stationary Phases for Liquid and Gas Chromatographic Separations?

Cui, Yong,Jia, Wenyan,Li, Yanan,Yu, Ziyun,Yuan, Chen,Yuan, Li-Ming,Zi, Min

, p. 891 - 900 (2022/02/03)

High-performance liquid chromatography (HPLC) and gas chromatography (GC) over chiral stationary phases (CSPs) represent the most popular and highly applicable technology in the field of chiral separation, but there are currently no CSPs that can be used for both liquid and gas chromatography simultaneously. We demonstrate here that two olefin-linked covalent organic frameworks (COFs) featuring chiral crown ether groups can be general CSPs for extensive separation not only in GC but also in normal-phase and reversed-phase HPLC. Both COFs have the same 2D layered porous structure but channels of different sizes and display high stability under different chemical environments including water, organic solvents, acids, and bases. Chiral crown ethers are periodically aligned within the COF channels, allowing for enantioselective recognition of guest molecules through intermolecular interactions. The COF-packed HPLC and GC columns show excellent complementarity and each affords high resolution, selectivity, and durability for the separation of a wide range of racemic compounds, including amino acids, esters, lactones, amides, alcohols, aldehydes, ketones, and drugs. The resolution performances are comparable to and the versatility is superior to those of the most widely used commercial chiral columns, showing promises for practical applications. This work thus advances COFs with high stability as potential universal CSPs for chromatography that are otherwise hard or impossible to produce.

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