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191664-14-9

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191664-14-9 Usage

General Description

Boc-(R)-2-(aminomethyl)-3-methylbutanoic acid, also known as Boc-aminomethylvaline, is a chemical compound commonly used in peptide synthesis and drug development. It is a derivative of valine and is often employed in the production of biologically active peptides due to its ability to enhance peptide stability and bioavailability. Boc-aminomethylvaline is a key building block for the creation of peptide-based pharmaceuticals and has been studied for its potential therapeutic applications in the treatment of various diseases and medical conditions. Its unique structure and functional properties make it an important component in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 191664-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,6,6 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 191664-14:
(8*1)+(7*9)+(6*1)+(5*6)+(4*6)+(3*4)+(2*1)+(1*4)=149
149 % 10 = 9
So 191664-14-9 is a valid CAS Registry Number.

191664-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-3-methyl-2-[[(2-methylpropan-2-yl)oxycarbonylamino]methyl]butanoic acid

1.2 Other means of identification

Product number -
Other names (2S)-2-{[(tert-Butoxycarbonyl)amino]methyl}-3-methylbutyric acid

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:191664-14-9 SDS

191664-14-9Relevant articles and documents

β2- And β3-Peptides with Proteinaceous Side Chains: Synthesis and Solution Structures of Constitutional Isomers, a Novel Helical Secondary Structure and the Influence of Solvation and Hydrophobic Interactions on Folding

Seebach, Dieter,Abele, Stefan,Gademann, Karl,Guichard, Gilles,Hintermann, Tobias,Jaun, Bernhard,Matthews, Jennifer L.,Schreiber, Juerg V.,Oberer, Lukas,Hommel, Ulrich,Widmer, Hans

, p. 932 - 982 (2007/10/03)

Enantiomerically pure β-amino-acid derivatives with the side chains of Ala, Val, and Leu in the 2- or 3-position (β2- and β3-amino acids, resp.), as well as with substituents in both the 2- and 3-positions (β2,3-amino acids, of like-configuration) have been prepared (compounds 8-17) and incorporated (by stepwise synthesis and fragment coupling, intermediates 24-34) into β-hexa-, β-hepta-, and β-dodecapeptides (1-17). The new and some of the previously prepared β-peptides (35-39) showed NH/ND exchange rates (in MeOH at room temperature) with τ1/2 values of up to 60 days, unrivalled by short chain α-peptides. All β-peptides 1-7 were designed to be able to attain the previously described 31-helical structure (Figs. 1 and 2). CD Measurements (Fig. 4), indicating a new secondary structure of certain β-peptides constructed of β2- and β3-amino acids, were confirmed by detailed NMR solution-structure analyses: a β2-heptapeptide (2c) and a β2,3-hexapeptide (7c) have the 31-helical structure (Figs. 6 and 7), while to a β2/β3-hexapeptide (4) with alternating substitution pattern H-(β2-Xaa-β3-Xaa)3-OH a novel, unusual helical structure (in (D5)pyridine, Fig. 8; and in CD3OH, Figs. 9 and 10) was assigned, with a central ten-membered and two terminal twelve-membered H-bonded rings, and with C=O and N-H bonds pointing alternatively up and down along the axis of the helix (Fig. 11). Thus, for the first time, two types of β-peptide turns have been identified in solution. Hydrophobic interactions of and hindrance to solvent accessibility by the aliphatic side chains are discussed as possible factors influencing the relative stability of the two types of helices.

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