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"Benzyl 6-(6-(benzyloxycarbonylamino)hexanamido)hexanoate" is a complex organic compound with the molecular formula C27H36N2O5. It is a derivative of benzyl ester, featuring a hexanoic acid chain with an amide group at the 6th position, which is further connected to another hexanamido chain through a benzyloxycarbonyl group. benzyl 6-(6-(benzyloxycarbonylamino)hexanamido)hexanoate is characterized by its long-chain structure and the presence of multiple amide linkages, which contribute to its unique chemical properties. It is often used in the synthesis of pharmaceuticals and other organic compounds due to its ability to form stable intermediates in peptide synthesis. The benzyl group serves as a protecting group for the amide, which can be removed under specific conditions to reveal the free amide group, a common strategy in organic synthesis to control reactivity and protect functional groups.

2899-61-8

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2899-61-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2899-61-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2899-61:
(6*2)+(5*8)+(4*9)+(3*9)+(2*6)+(1*1)=128
128 % 10 = 8
So 2899-61-8 is a valid CAS Registry Number.

2899-61-8Relevant academic research and scientific papers

In situ formation of N-trifluoroacetoxy succinimide (TFA-NHS): One-pot formation of succinimidyl esters, N-trifluoroacetyl amino acid succinimidyl esters, and N-maleoyl amino acid succinimidyl esters

Leonard, Nicholas M.,Brunckova, Jarmila

experimental part, p. 9169 - 9174 (2011/12/16)

A method for the in situ formation of N-trifluoroacetoxy succinimide (TFA-NHS) and its application in the formation of succinimidyl esters is presented. The developed method provides N-trifluoroacetyl and N-maleoyl amino acid succinimidyl esters from a variety of amino acids using a one-pot, high-yielding protocol. Investigations into the formation of an N-maleoyl amino acid succinimidyl ester supported the proposal of a revised reaction mechanism, and contributed to the optimization of the reaction conditions.

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