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N-trityl-glycine diethylamine salt is a chemical compound with the molecular formula C23H24N2O2. It is a derivative of glycine, an amino acid, where the amino group is substituted with a trityl group (a phenylmethyl group). The diethylamine salt form indicates that the compound has been protonated with diethylamine, resulting in a positively charged species. N-trityl-glycine ; diethylamine salt is often used in organic synthesis and as a reagent in various chemical reactions due to its unique properties. It is known for its stability and can be used in the preparation of other complex organic molecules. The trityl group provides a bulky, electron-rich environment that can influence the reactivity and selectivity of the molecule in chemical transformations.

3226-93-5

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3226-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3226-93-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,2 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3226-93:
(6*3)+(5*2)+(4*2)+(3*6)+(2*9)+(1*3)=75
75 % 10 = 5
So 3226-93-5 is a valid CAS Registry Number.

3226-93-5Downstream Products

3226-93-5Relevant academic research and scientific papers

TRITYLATION REACTIONS BASED ON METALLIC CATALYSIS

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Page/Page column 21-22, (2010/11/25)

The invention relates to a method for preparing tritylated compounds in which protic functional groups are protected with the triphenylmethyl group, method based on the homogeneous catalysis exercised by salts or metal complexes in organic solvents. The invention relates in particular to a method for the selective tritylation of some groups, obtained both directly and by selective detritylation, with methods based on metallic catalysis. The application to amino acids, typical substrates not suitable to be subjected as such to homogeneous tritylations in organic solvents, indicates the ability of the method to extend also to hydrophilic substrates. The method allows to obtain with high yield pertrityl amino acids, N-tritylamino acids or amino acids tritylated only in lateral chain, compounds which heretofore were either difficult to obtain in aqueous solvents or obtainable through indirect methods. All, in any case, are important intermediates in peptide synthesis.

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