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Alanine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl]-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69872-65-7

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69872-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69872-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,7 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69872-65:
(7*6)+(6*9)+(5*8)+(4*7)+(3*2)+(2*6)+(1*5)=187
187 % 10 = 7
So 69872-65-7 is a valid CAS Registry Number.

69872-65-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[(2S)-3-(4-hydroxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoyl]amino]-2-methylpropanoic acid

1.2 Other means of identification

Product number -
Other names Alanine,N-[N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl]-2-methyl

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:69872-65-7 SDS

69872-65-7Relevant academic research and scientific papers

A new peptide motif in the formation of supramolecular double helices

Jana, Poulami,Maity, Sibaprasad,Maity, Suman Kumar,Haldar, Debasish

, p. 2092 - 2094 (2011/04/14)

The single crystal X-ray diffraction studies of a new tripeptide motif Boc-Tyr-Aib-Xaa-OMe (Xaa = Leu/Ile/Ala) reveal that the peptides adopt β-turn conformations which self-assemble to form a supramolecular double helical structure using various non-covalent interactions in the solid state and the peptides exhibit a type-III N2 sorption isotherm.

Insights into self-assembling nanoporous peptide and in situ reducing agent

Jana, Poulami,Maity, Sibaprasad,Haldar, Debasish

, p. 973 - 978 (2012/02/01)

A tripeptide containing an Aib (α-amino isobutyric acid) residue self-assembles to form porous nanomaterials in solid state. In spite of having a hollow nanotubular structure, the self-assembly nature of the peptide is different, which leads to the formation of pores with different internal diameters. The single-crystal X-ray diffraction study reveals that the peptide forms continuous hydrogen-bonded poly-disperse nanopores (3, 5 and 8 membered) starting from the β-turn conformation as an associating sub-unit. The field emission scanning electron micrograph (FESEM) shows that the average pore sizes are in the range of 20 to 200 nm, although a few large pores are also visible. Moreover, the peptide 1 acts as an in situ reducing agent to synthesize hexagonal gold nanoparticles (GNP).

A mechanistic and kinetic study of the formation of metal nanoparticles by using synthetic tyrosine-based oligopeptides

Si, Satyabrata,Bhattacharjee, Rama Ranjan,Banerjee, Arindam,Mandal, Tarun K.

, p. 1256 - 1265 (2008/09/18)

Synthetic oligopeptides containing redox-active tyrosine residues have been employed to prepare gold and silver nanoparticles. In this reduction process an electron from the tyrosinate ion of the peptide is transferred to the metal ion at basic pH through the formation of a tyrosyl radical, which is eventually converted to its dityrosine form during the reaction. This reaction mechanism was confirmed from UV-visible, fluorescence, and EPR spectroscopy and was found to be pH-dependent. Transmission electron microscopy measurement shows that the average size and the monodispersity of gold nanoparticles increase as the number of tyrosine residues in the peptide increases. The kinetic study, based on spectrophotometric measurements of the surface plasmon resonance optical property, shows that the rate of formation of gold nanoparticles was much faster at higher pH than at lower pH and was also dependent on the number of tyrosine residues present in the peptide. The dityrosine form of the peptide was found to retain reducing properties like those of tyrosine in basic medium.

Investigation of the structural parameters involved in the μ and δ opioid receptor discrimination of linear enkephalin-related peptides

Gacel,Zajac,Delay-Goyet,Dauge,Roques

, p. 374 - 383 (2007/10/02)

The previous rules proposed for selective recognition of μ and δ opioid receptors by modified enkephalins were investigated through an extensive structure-activity study. Thus, modifications of the sequence of TRIMU 4 (Tyr-D-Ala-Gly-NHCH(CH3)CH

Novel Analogues of Enkephalin: Identification of Functional Groups Required for Biological Activity

Gorin, Fredric A.,Balasubramanian, T. M.,Cicero, Theodore J.,Schwietzer, John,Marshall, Garland R.

, p. 1113 - 1122 (2007/10/02)

Novel tri- and tetrapeptide analogues of enkephalin, in conjunction with earlier structure-activity data, confirm that chemical substituents present in the first and fourth residues of enkephalin are required for in vitro biological activity.A class of ar

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