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"Z-Tyr(CH2Ph)-Gly-NH-NH-Boc" is a complex organic compound that serves as a peptide building block. It is composed of a tyrosine (Tyr) residue, which is a naturally occurring amino acid, with a phenyl group (Ph) attached to its side chain. This phenyl group is connected through a methylene bridge (CH2). The compound also includes a glycine (Gly) residue, which is the simplest amino acid. The "NH-NH" part indicates the presence of a peptide bond, which links the two amino acids. The "Boc" group, or tert-butyloxycarbonyl, is a protecting group used in peptide synthesis to prevent unwanted side reactions, particularly during the coupling of amino acids. Z-Tyr(CH2Ph)-Gly-NH-NH-Boc is a key intermediate in the synthesis of larger peptides and proteins, where the Boc group can be removed under acidic conditions to allow further reactions.

51952-35-3

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51952-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51952-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,5 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51952-35:
(7*5)+(6*1)+(5*9)+(4*5)+(3*2)+(2*3)+(1*5)=123
123 % 10 = 3
So 51952-35-3 is a valid CAS Registry Number.

51952-35-3Downstream Products

51952-35-3Relevant academic research and scientific papers

Process for preparing the releasing hormone of luteinizing hormone (LH) and of follicle stimulating hormone (FSH), salts and compositions thereof, and intermediates therefor

-

, (2008/06/13)

A process for preparing the LH- and FSH-releasing hormone of the formula I which is isolated as the hydrochloride salt and optionally converted to other pharmaceutically acceptable salts or to pharmaceutically acceptable metal complexes.

Luteinizing hormone releasing hormone and analogs. Synthesis and biological activity

Immer,Nelson,Revesz,Sestanj,Goetz

, p. 1060 - 1065 (2007/10/05)

A fragment synthesis of LH RH is described which lends itself to large scale preparation. Fragment 1-3 is coupled with fragment 4-6 followed by reaction with the tetrapeptide 7-10 to yield the unprotected decapeptide. The preparation of analogs follows the same synthetic pattern. The biological activity of the analogs is compared with that of synthetic LH RH.

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