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640281-39-6

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640281-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 640281-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,0,2,8 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 640281-39:
(8*6)+(7*4)+(6*0)+(5*2)+(4*8)+(3*1)+(2*3)+(1*9)=136
136 % 10 = 6
So 640281-39-6 is a valid CAS Registry Number.

640281-39-6Relevant academic research and scientific papers

Environmentally Friendly SPPS II: Scope of Green Fmoc Removal Protocol Using NaOH and Its Application for Synthesis of Commercial Drug Triptorelin

P?ibylka, Adam,Krchňák, Viktor,Schütznerová, Eva

, p. 8798 - 8811 (2020/09/09)

With the growing necessity to consider environmental impacts when synthesizing peptide-based drugs and to expand upon the recently published short communication report, we herein present a thorough evaluation of a green Fmoc removal protocol. Our protocol avoids the use of hazardous components (using piperidine as a base and dichloromethane (DCM) and N,N-dimethylformamide (DMF) as solvents) and relies on the utilization of the green mineral base NaOH in combination with the greener solvent 2-methyltetrahydrofuran (2-MeTHF) mixed with MeOH. For the original Fmoc removal cocktail (solvents ratio of 1:1), we evaluated the impact of quality/purity of the used 2-MeTHF, scale-up, ratio of 2-MeTHF/MeOH, utilized hydroxide, temperature, and reaction time. An alternative 3:1 protocol was examined using various amino acids, and only Gly required the optimization of the Fmoc removal cocktail composition. The optimized protocol used to remove Fmoc from Gly residue was proved by the synthesis of Leu-enkephalin. We also investigated the stability of the conventional amino acid side-chain-protecting groups, t-Bu, Boc, Trt, and Pbf, and the formation of aspartimide as an undesirable side reaction that occurs during Fmoc solid-phase peptide synthesis (SPPS). The applicability of this synthesis strategy was documented by evaluating the SPPS of a commercial drug used for prostate and breast cancer treatments - decapeptide triptorelin.

A Concise and Flexible Total Synthesis of (-)-Diazonamide A

Burgett, Anthony W. G.,Li, Qingyi,Wei, Qi,Harran, Patrick G.

, p. 4961 - 4966 (2007/10/03)

The remarkable action of an IIII species on a tripeptide containing acyclic tyrosine/ tryptophan is the key step in a total synthesis of (-)-diazonamide A. The completed preparation of this new antimitotic is concise, multiply convergent, and a

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