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1075-62-3

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1075-62-3 Usage

General Description

N-(6-aminopyridin-2-yl)acetamide is a chemical compound with the molecular formula C7H9N3O. It is an amide derivative of 6-aminopyridine, which is a heterocyclic organic compound containing a pyridine ring with an amino group at the 6-position. N-(6-aminopyridin-2-yl)acetamide is commonly used in the pharmaceutical industry as a building block in the synthesis of various bioactive compounds, such as pharmaceutical drugs and agrochemicals. It has also been studied for its potential therapeutic applications, including its use in treating neurological disorders and as an analgesic. Additionally, it has been investigated for its potential as a corrosion inhibitor in industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1075-62-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1075-62:
(6*1)+(5*0)+(4*7)+(3*5)+(2*6)+(1*2)=63
63 % 10 = 3
So 1075-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H9N3O/c1-5(11)9-7-4-2-3-6(8)10-7/h2-4H,1H3,(H3,8,9,10,11)

1075-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(6-Aminopyridin-2-yl)acetamide

1.2 Other means of identification

Product number -
Other names N-(6-aminopyridin-2-yl)acetamide

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:1075-62-3 SDS

1075-62-3Relevant articles and documents

Dictating Nanoparticle Assembly via Systems-Level Control of Molecular Multivalency

Santos, Peter J.,Cao, Zhen,Zhang, Jianyuan,Alexander-Katz, Alfredo,Macfarlane, Robert J.

, p. 14624 - 14632 (2019)

Nanoparticle assembly can be controlled by multivalent binding interactions between surface ligands, indicating that more precise control over these interactions is important to design complex nanoscale architectures. It has been well-established in natural materials that the arrangement of different molecular species in three dimensions can affect the ability of individual supramolecular units to coordinate their binding, thereby regulating the strength and specificity of their collective molecular interactions. However, in artificial systems, limited examples exist that quantitatively demonstrate how changes in nanoscale geometry can be used to rationally modulate the thermodynamics of individual molecular binding interactions. As a result, the use of nanoscale design features to regulate molecular bonding remains an underutilized design handle to control nanomaterials synthesis. Here we demonstrate a polymer-coated nanoparticle material where supramolecular bonding and nanoscale structure are used in conjunction to dictate the thermodynamics of their multivalent interactions, resulting in emergent bundling of supramolecular binding groups that would not be expected on the basis of the molecular structures alone. Additionally, we show that these emergent phenomena can controllably alter the superlattice symmetry by using the mesoscale particle arrangement to alter the thermodynamics of the supramolecular bonding behavior. The ability to rationally program molecular multivalency via a systems-level approach therefore provides a major step forward in the assembly of complex artificial structures, with implications for future designs of both nanoparticle- and supramolecular-based materials.

Reinforcing Supramolecular Bonding with Magnetic Dipole Interactions to Assemble Dynamic Nanoparticle Superlattices

Santos, Peter J.,Macfarlane, Robert J.

, p. 1170 - 1174 (2020)

Assembling superparamagnetic particles into ordered lattices is an attractive means of generating new magnetically responsive materials, and is commonly achieved by tailoring interparticle interactions as a function of the ligand coating. However, the inherent linkage between the collective magnetic behavior of particle arrays and the assembly processes used to generate them complicates efforts to understand and control material synthesis. Here, we use a synergistic combination of a chemical force (hydrogen bonding) and magnetic dipole coupling to assemble polymer-brush coated superparamagnetic iron oxide nanoparticles, where the relative strengths of these interactions can be tuned to reinforce one another and stabilize the resulting superlattice phases. We find that we can precisely control both the dipole-dipole coupling between nanoparticles and the strength of the ligand-ligand interactions by modifying the interparticle spacing through changes to the polymer spacer between the hydrogen bonding groups and the nanoparticles' surface. This results in modulation of the materials' blocking temperature, as well as the stabilization of a unique superlattice phase that only exists when magnetic coupling between particles is present. Using magnetic interactions to affect nanoparticle assembly in conjunction with ligand-mediated interparticle interactions expands the potential for synthesizing predictable and controllable nanoparticle-based magnetic composites.

METALLO-BETA-LACTAMASE INHIBITORS

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Page/Page column 66, (2017/04/04)

The present invention relates to compounds of formula I that are metallo-β-lactamase inhibitors, the synthesis of such compounds, and the use of such compounds for use with β-lactam antibiotics for overcoming resistance.

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