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The chemical compound in question, (S)-1-[(S)-1-((1S,2S)-1-hydrazinocarbonyl-2-methyl-butylcarbamoyl)-2-phenyl-ethylcarbamoyl]-ethyl-carbamic acid tert-butyl ester, is a complex organic molecule with a molecular formula of C22H38N4O4. It is a chiral compound, meaning it has a non-superimposable mirror image, and it is a derivative of carbamic acid. The compound features a hydrazinocarbonyl group, a carbamoyl group, and a tert-butyl ester group, which contribute to its unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research. Its structure is characterized by a series of chiral centers and functional groups that make it a versatile building block for the synthesis of more complex molecules.

3081-44-5

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3081-44-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3081-44-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,8 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3081-44:
(6*3)+(5*0)+(4*8)+(3*1)+(2*4)+(1*4)=65
65 % 10 = 5
So 3081-44-5 is a valid CAS Registry Number.

3081-44-5Downstream Products

3081-44-5Relevant academic research and scientific papers

Polymer-Bound Oxime Esters as Supports for Solid-Phase Peptide Synthesis. Preparation of Protected Peptide Fragments.

DeGrado, William F.,Kaiser, Emil Thomas

, p. 1295 - 1300 (1980)

A series of polystyrene-bound substituted benzophenone oximes (II) have been synthesized and tested as potential supports for the solid-phase preparation of protected peptide fragments.The polymer-bound p-nitrobenzophenone oxime (IID) has been found to be a suitable support for stepwise peptide synthesis.Protected peptides can be assembled on IID by coupling and deprotection steps similar to those employed in the usual Merrifield solid-phase procedures.Cleavage of peptides from IID can be accomplished with hydrazine and amino acid esters under mild conditionswhich do not affect benzyl ester side-chain protecting groups.The utility of IID has been illustrated in the synthesis of protected peptide hydrazides and esters, several of which have aspartic and glutamic acid side chains protected by benzyl groups.

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