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109792-60-1

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109792-60-1 Usage

Description

tert-Butyl (12-aminododecyl)carbamate can be used as a PROTAC linker in the synthesis of PROTACs. tert-Butyl (12-aminododecyl)carbamate is an alkane chain with terminal amine and Boc-protected amino groups. Amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine.

Uses

12-(tert-Butoxycarbonylamino)dodecylamine can be used to synthesize inhibitors of topoisomerase I for use as anticancer agents.

Check Digit Verification of cas no

The CAS Registry Mumber 109792-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,7,9 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 109792-60:
(8*1)+(7*0)+(6*9)+(5*7)+(4*9)+(3*2)+(2*6)+(1*0)=151
151 % 10 = 1
So 109792-60-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H36N2O2/c1-17(2,3)21-16(20)19-15-13-11-9-7-5-4-6-8-10-12-14-18/h4-15,18H2,1-3H3,(H,19,20)

109792-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BOC-1,12-DIAMINODODECANE

1.2 Other means of identification

Product number -
Other names Boc-DADdec

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:109792-60-1 SDS

109792-60-1Relevant articles and documents

A new perylene bisimide bola amphiphile: Synthesis, characterization, fluorescent properties and applications as a potential probe

Franceschin, Marco,Bombelli, Cecilia,Borioni, Silvia,Bozzuto, Giuseppina,Eleuteri, Silvia,Mancini, Giovanna,Molinari, Agnese,Bianco, Armandodoriano

, p. 2166 - 2173 (2013)

Fluorescently-tagged lipids are a powerful tool for investigating the dynamics of lipids in cell biological studies and in biophysical applications. Herein we report the synthesis and the characterization of a new bola amphiphile, PC12, based on a bisimidic perylene moiety: a central perylene unit is symmetrically linked to two aliphatic chains both ending with a quaternary ammonium group. Absorption and fluorescent properties of the newly synthesized compound were investigated in DMSO and in water as a function of concentration and temperature. Further, the entrapment efficiency, the fluorescence behavior in dimyristoyl-sn-glycero-phosphocholine (DMPC) liposomes, and cell uptake on human and murine glioblastoma cell lines were evaluated. When loaded in liposomes, PC12 follows the same destiny of liposomes themselves in the cell cultures: this is an interesting result because PC12 could be used both as an aspecific dye (free form) and as an organelle-specific lipid probe.

Solvent-dependent self-assembly and morphological transition of low-molecular-weight azobenzene organogel

Zhang, Zhiwei,Zhang, Shaoze,Zhang, Junji,Zhu, Liangliang,Qu, Dahui

, p. 4891 - 4895 (2017)

A novel low molecular weight organogelator (LMOG) containing an azobenzene group has been designed and synthesized. Stable gels could be formed in various organic solvents. UV–Vis spectroscopy indicated that the sol-gel transition of the organogels could be reversibly tuned by UV/visible light irradiations. Importantly, scanning electron microscopy (SEM) revealed that the characteristic gelation morphologies would vary from solvents of different polarities. FT-IR, XRD and rheological measurements demonstrated that the different nanostructures in polar and non-polar solvents might result from the differences in the intermolecular hydrogen bonding, π-π stacking driving forces as well as the different stacking models for the formation of the gels. Moreover, as an efficient phase-selective gelator, this photo-switchable gel could perform as an efficient absorbent and water cleaner to remove pollutants (e.g. rhodamine B).

Investigation of the lactam side chain length necessary for optimal indenoisoquinoline topoisomerase I inhibition and cytotoxicity in human cancer cell cultures

Morrell, Andrew,Placzek, Michael S.,Steffen, Jamin D.,Antony, Smitha,Agama, Keli,Pommier, Yves,Cushman, Mark

, p. 2040 - 2048 (2007)

Indenoisoquinolines with lactam substituents such as ethylamino, propylamino, and butylamino have previously demonstrated potent biological activity, but an optimal length has never been established. In the present study, a series of simplified indenoisoquinoline analogues possessing a linker spacing of 0-12 carbon atoms between the lactam nitrogen and the terminal amino group have been prepared, determining that 2-4-atom lengths are optimal for topoisomerase I inhibition and cytotoxicity. Using these lengths, analogues were prepared with the amino group and portions of the linker replaced by a pyridine ring. A three-carbon spacer within the pyridine series still demonstrated potent topoisomerase I inhibition.

Efficient phosphodiester cleaving nanozymes resulting from multivalency and local medium polarity control

Diez-Castellnou, Marta,Mancin, Fabrizio,Scrimin, Paolo

supporting information, p. 1158 - 1161 (2014/02/14)

The self-organization of Zn(II) complexes on the surface of 1.6-nm diameter gold nanoparticles (nanozymes) allows the spontaneous formation of multiple bimetallic catalytic sites capable to promote the cleavage of a RNA model substrate. We show that by tu

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