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Tert-Butyl 2-amino-5-methylhexanoate is a synthetic compound with the chemical formula C9H19NO2. It is a derivative of the amino acid valine, featuring a tert-butyl group attached to the amino group. This colorless liquid with a mild odor is soluble in organic solvents such as ethanol and acetone, and it serves as a versatile reagent in organic synthesis and a building block in pharmaceutical research.

1543874-84-5

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1543874-84-5 Usage

Uses

Used in Pharmaceutical Research:
Tert-Butyl 2-amino-5-methylhexanoate is used as a building block for the development of new pharmaceuticals, leveraging its unique chemical structure to create novel drug candidates.
Used in Organic Synthesis:
As a reagent, Tert-Butyl 2-amino-5-methylhexanoate is utilized in various organic synthesis processes, contributing to the creation of a wide array of chemical compounds.
Used in Agrochemical Production:
Tert-Butyl 2-amino-5-methylhexanoate is employed in the production of agrochemicals, where its properties can be harnessed to develop new pesticides or other agricultural products.
Used in Other Industries:
tert-Butyl 2-amino-5-methylhexanoate's versatility extends to other industries, where it may be used for specific applications that benefit from its chemical properties, such as in the development of new materials or chemical intermediates.

Check Digit Verification of cas no

The CAS Registry Mumber 1543874-84-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,4,3,8,7 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1543874-84:
(9*1)+(8*5)+(7*4)+(6*3)+(5*8)+(4*7)+(3*4)+(2*8)+(1*4)=195
195 % 10 = 5
So 1543874-84-5 is a valid CAS Registry Number.

1543874-84-5Downstream Products

1543874-84-5Relevant academic research and scientific papers

N-Arylation of Amino Acid Esters to Expand Side Chain Diversity in Ketoxime Peptide Ligations

Young, Hailey A.,Guthrie, Quibria A. E.,Proulx, Caroline

, p. 1748 - 1755 (2020)

Palladium-catalyzed N-arylations of amino acid tert-butyl esters using 4-bromo-N,N-dimethylaniline as a coupling partner are reported. The resulting N-aryl amino acid esters are suitable building blocks for the synthesis of electron-rich N-aryl peptides, which undergo oxidative couplings to aminooxy groups to afford ketoxime peptides under mild conditions. N-aryl amino acid tert-butyl esters possessing unnatural side chains were also accessed via glycine Schiff base alkylation, further increasing the scope of Cα-substitution in ketoxime peptides.

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