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{[(Carbobenzyloxy)glycyl]glycyl}glycine tert-butyl ester is a complex organic compound with the molecular formula C26H37N2O7. It is a peptide derivative, consisting of a glycine residue with a carbobenzyloxy (Cbz) protecting group, another glycine residue, and a final glycine residue with a tert-butyl (t-Bu) ester group. {[(carbobenzyloxy)glycyl]glycyl}glycine tert-butyl ester is often used in peptide synthesis as a building block, where the Cbz group serves to protect the amino group during the coupling process, and the t-Bu ester group protects the carboxylic acid group. The compound is crucial in the synthesis of larger peptides and proteins, as it allows for the stepwise assembly of peptide chains with controlled reactivity and selectivity.

7521-91-7

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7521-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7521-91-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,2 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7521-91:
(6*7)+(5*5)+(4*2)+(3*1)+(2*9)+(1*1)=97
97 % 10 = 7
So 7521-91-7 is a valid CAS Registry Number.

7521-91-7Relevant academic research and scientific papers

CYTOTOXIC BENZODIAZEPINE DERIVATIVES

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Paragraph 0450, (2016/04/19)

The invention relates to novel benzodiazepine derivatives with antiproliferative activity and more specifically to novel benzodiazepine compounds of formula (I)-(VI). The invention also provides conjugates of the benzodiazepine compounds linked to a cell-binding agent. The invention further provides compositions and methods useful for inhibiting abnormal cell growth or treating a proliferative disorder in a mammal using the compounds or conjugates of the invention.

An approach to nanobioparticles - Synthesis and characterization of fulleropeptides

Bjelakovic, Mira,Todorovic, Nina,Milic, Dragana

, p. 5291 - 5300 (2012/10/29)

Two sets of new peptides incorporating fulleropyrrolidine units - Fp-GABAn-Glym-OtBu - have been designed, synthesized and completely characterized. In the first series the chain contained only GABA (γ-aminobutyric) residues, whereas in the second one glycine moieties were also inserted as well as GABA. Most of the target compounds were prepared by DCC/DMAP-assisted coupling of previously synthesized GABA-containing fulleropyrrolidinic acid and corresponding C-protected small peptides, although for two fulleropeptides [3+2] cycloadditions of azomethine ylides to C 60 were employed. All new compounds were characterized by standard spectroscopic methods. Complete assignments of peptide spin systems were achieved by extensive NMR analysis (1H, 13C, H,H-COSY, HSQC, HMBC and TOCSY). Copyright

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