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N2-benzyloxycarbonyl-L-glutamine hydrazide is a synthetic chemical compound with the molecular formula C14H18N4O4. It is a derivative of L-glutamine, an amino acid, where the carboxylic acid group is protected with a benzyloxycarbonyl (Cbz) group, and the amino group is replaced by a hydrazide group. N2-benzyloxycarbonyl-L-glutamine hydrazide is often used in peptide synthesis as a protecting group for the carboxylic acid function, allowing for the selective coupling of amino acids during the assembly of peptide chains. The hydrazide group can be used for further functionalization or as a leaving group in certain chemical reactions. It is a white crystalline solid and is soluble in common organic solvents. Due to its reactivity and potential to form hazardous decomposition products, it is important to handle N2-benzyloxycarbonyl-L-glutamine hydrazide with care, following appropriate safety protocols.

4008-03-1

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4008-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4008-03-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,0 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4008-03:
(6*4)+(5*0)+(4*0)+(3*8)+(2*0)+(1*3)=51
51 % 10 = 1
So 4008-03-1 is a valid CAS Registry Number.

4008-03-1Relevant academic research and scientific papers

Combinatorial synthesis of 3,5-Dimethylene substituted 1,2,4-Triazoles

Woodard, Scott S.,Jerome, Kevin D.

, p. 132 - 137 (2012/04/18)

Combinatorial cyclizations of imidates and hydrazides with methylene linked R groups, generated from the corresponding nitriles and carboxylic acids, respectively, provided a large library of 3,5-dimethylene substituted 1,2,4- trizoles. 2011 Bentham Science Publishers Ltd.

Fast and convenient synthesis of α-N-protected amino acid hydrazides

Verardo, Giancarlo,Geatti, Paola,Lesa, Barbara

, p. 559 - 564 (2007/10/03)

A fast, simple and convenient synthesis of α-N-protected amino acid hydrazides is reported. The procedure involves the reaction between hydrazine monohydrate and the mixed anhydride obtained from an α-N-protected amino acid and ethyl chloroformate. When m

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