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Carbamic acid, [2-(octylamino)-2-oxo-1-(phenylmethyl)ethyl]-, 1,1-dimethylethyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105329-20-2

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105329-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105329-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,2 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 105329-20:
(8*1)+(7*0)+(6*5)+(5*3)+(4*2)+(3*9)+(2*2)+(1*0)=92
92 % 10 = 2
So 105329-20-2 is a valid CAS Registry Number.

105329-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name BOC-L-phenylalanine octylamide

1.2 Other means of identification

Product number -
Other names -

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:105329-20-2 SDS

105329-20-2Relevant academic research and scientific papers

An example of green surfactant systems based on inherently biodegradable IL-derived amphiphilic oximes

Gathergood, Nicholas,Ghosh, Kallol K.,Kapitanov, Illia V.,Karpichev, Yevgen,Pandya, Subhashree Jayesh,Sahu, Reshma,Sinha, Deepak,Usmani, Zeba

, (2020)

Progress in the development of biodegradable ionic liquids (ILs) leads to designing green surfactant formulations for miscellaneous applications. In this work, we present synthesis of a series of novel IL-derived amphiphilic pyridinium oximes composed by

Antimicrobial and antitumor activity of peptidomimetics synthesized from amino acids

Li, Huan,Fu, Shuang,Wang, Yudan,Yuan, Xuan,Liu, Lijia,Dong, Hongxing,Wang, Qiang,Zhang, Zhijia

, (2020/12/07)

Thirteen cationic peptidomimetics derived from amino acids bearing an alkyl or ethynylphenyl moiety that mimic the structure of cationic antibacterial peptides were designed and synthesized using a simple coupling reaction of an amino acid with a substitu

Carbon-Nanotube-Mediated Electrochemical Transition in a Redox-Active Supramolecular Hydrogel Derived from Viologen and an l -Alanine-Based Amphiphile

Datta, Sougata,Bhattacharya, Santanu

, p. 7524 - 7532 (2016/05/24)

A two-component hydrogelator (16-A)2-V2+, comprising an l-alanine-based amphiphile (16-A) and a redox-active viologen based partner (V2+), is reported. The formation the hydrogel depended, not only on the acid-to-amine stoichiometric ratio, but on the choice of the l-amino acid group and also on the hydrocarbon chain length of the amphiphilic component. The redox responsive property and the electrochemical behavior of this two-component system were further examined by step-wise chemical and electrochemical reduction of the viologen nucleus (V2+/V+ and V+/V0). The half-wave reduction potentials (E1/2) associated with the viologen ring shifted to more negative values with increasing amine component. This indicates that higher extent of salt formation hinders reduction of the viologen moiety. Interestingly, the incorporation of single-walled carbon nanotubes in the electrochemically irreversible hydrogel (16-A)2-V2+ transformed it into a quasi-reversible electrochemical system.

Novel dendrimeric lipopeptides with antifungal activity

Janiszewska, Jolanta,Sowińska, Marta,Rajnisz, Aleksandra,Solecka, Jolanta,?cka, Izabela,Milewski, S?awomir,Urbańczyk-Lipkowska, Zofia

scheme or table, p. 1388 - 1393 (2012/04/04)

A series of new cationic lipopeptides containing branched, amphiphilic polar head derived from (Lys)Lys(Lys) dendron and C8 or C 12 chain at C-end were designed, synthesized and characterized. Antimicrobial in vitro activity expresse

Water-compatible iminium activation: Highly enantioselective organocatalytic michael addition of malonates to α,β-unsaturated enones

Mao, Zhifeng,Jia, Yaomei,Li, Wenyi,Wang, Rui

supporting information; experimental part, p. 7428 - 7430 (2011/02/22)

The highly enantioselective Michael addition of malonates to α,β-unsaturated ketones in water was reported to be catalyzed by a primary-secondary diamine catalyst containing a long alkyl chain. This asymmetric Michael addition process was found to be effe

C3-Symmetric, amino acid based organogelators and thickeners: a systematic study of structure-property relations

de Loos, Maaike,van Esch, Jan H.,Kellogg, Richard M.,Feringa, Ben L.

, p. 7285 - 7301 (2008/02/05)

A class of C3-symmetric amino acid based organogelators and thickeners featuring a rigid core have been developed. Structural variation yielded a number of compounds, the aggregation behaviour and resulting aggregates and gels of which were studied by FTIR spectroscopy, dropping ball measurements, differential scanning calorimetry and transmission electron microscopy. These studies showed that the nature of the core unit, the type of hydrogen-bonding units and the applied amino acids have a strong influence on the interactions, resulting in large differences in aggregation properties, thermal stability and morphology between the various compounds. The results provide a basis for a better understanding of the relation between aggregate/gel properties and molecular structure. The structural variation available for these compounds allows fine-tuning of the gelators with respect to aggregation behaviour and gel properties.

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