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<3-(benzyloxy)-4-methyl-2-nitrobenzoyl>-L-threonyl-D-valyl-L-prolyl-sarcosine tert-butyl ester is a complex organic compound with a molecular formula of C31H40N2O10. It is a peptide-like molecule, consisting of a benzyloxy-protected nitrobenzoyl group, an L-threonine residue, a D-valine residue, an L-proline residue, and a sarcosine residue, with a tert-butyl ester group at the C-terminus. <3-(benzyloxy)-4-methyl-2-nitrobenzoyl>-L-threonyl-D-valyl-L-prolyl-sarcosine tert-butyl ester is of interest in the field of medicinal chemistry, particularly in the development of potential therapeutic agents, due to its unique structure and potential interactions with biological targets. The presence of the nitrobenzoyl group and the chiral amino acids (L-threonine, D-valine, and L-proline) contribute to its specific properties and potential applications in drug design.

6041-34-5

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6041-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6041-34-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,4 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6041-34:
(6*6)+(5*0)+(4*4)+(3*1)+(2*3)+(1*4)=65
65 % 10 = 5
So 6041-34-5 is a valid CAS Registry Number.

6041-34-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(benzyloxy)-4-methyl-2-nitrobenzoyl]-L-threonyl-D-valyl-L-prolyl-sarcosine tert-butyl ester

1.2 Other means of identification

Product number -
Other names N-(3-BzlO-4-Me-2-nitrobenzoyl)-Thr-D-Val-Pro-Sar-OtBu

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6041-34-5 SDS

6041-34-5Relevant academic research and scientific papers

Conformation and Dimerization of Actinomycin-Related Peptide Lactones in Solution and in the Solid State

Mauger, Anthony B.,Stuart, Oswald A.,Ferretti, James A.,Silverton, James V.

, p. 7154 - 7163 (2007/10/02)

Actinomycin-related peptide lactone derivatives with the amino acid sequences Thr-D-Val-Pro-Sar-MeVal and Thr-D-Val-Pro-Sar-MeAla and the corresponding actinomycins (actinomycin D and its novel 5,5'-MeAla analoque) were synthesized by a new route.The solution properties of these compounds were studied by proton NMR in chloroform and acetone solutions.In dry chloroform, two conformers, A and C, are found, the ratio of which was concentration-dependent and results from dimerization of the A conformer.An X-ray crystallographic investigation of a Thr-D-Val-Pro-Sar-MeAla derivative indicated that hydrogen-bond associated pairs of A conformers, with a juxtapositional geometry remarkably similar to that known for actinomycin, were present in the solid state.

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