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N-(6-Methyl-2-pyridyl)-4-aminobenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36845-08-6

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36845-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36845-08-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,4 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36845-08:
(7*3)+(6*6)+(5*8)+(4*4)+(3*5)+(2*0)+(1*8)=136
136 % 10 = 6
So 36845-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H13N3O/c1-9-3-2-4-12(15-9)16-13(17)10-5-7-11(14)8-6-10/h2-8H,14H2,1H3,(H,15,16,17)

36845-08-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-N-(6-methylpyridin-2-yl)benzamide

1.2 Other means of identification

Product number -
Other names BENZAMIDE,p-AMINO-N-(6-METHYL-2-PYRIDYL)

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:36845-08-6 SDS

36845-08-6Downstream Products

36845-08-6Relevant academic research and scientific papers

Molecular recognition: Chain length selectivity studies of dicarboxylic acids by the cavity of a new Troger's base receptor

Goswami, Shyamaprosad,Ghosh, Kumaresh

, p. 4503 - 4506 (1997)

A new dicarboxylic acid receptor 1 having two pyridine amide motifs built on a Troger's base spacer has been designed and synthesised. The binding studies are performed with a series or dicarboxylic acids and the cavity of receptor 1 was found to be selec

Compositional Persistence in a Multicyclic Network of Synthetic Replicators

Huck, Jürgen,Kosikova, Tamara,Philp, Douglas

, p. 13905 - 13913 (2019)

The emergence of collections of simple chemical entities that create self-sustaining reaction networks, embedding replication and catalysis, is cited as a potential mechanism for the appearance on the early Earth of systems that satisfy minimal definitions of life. In this work, a functional reaction network that creates and maintains a set of privileged replicator structures through auto- A nd cross-catalyzed reaction cycles is created from the pairwise combinations of four reagents. We show that the addition of individual preformed templates to this network, representing instructions to synthesize a specific replicator, induces changes in the output composition of the system that represent a network-level response. Further, we establish through sets of serial transfer experiments that the catalytic connections that exist between the four replicators in this network and the system-level behavior thereby encoded impose limits on the compositional variability that can be induced by repeated exposure to instructional inputs, in the form of preformed templates, to the system. The origin of this persistence is traced through kinetic simulations to the properties and inter-relationships between the critical ternary complexes formed by the auto- A nd crosscatalytic templates. These results demonstrate that in an environment where there is no continuous selection pressure the network connectivity, described by the catalytic relationships and system-level interactions between the replicators, is persistent, thereby limiting the ability of this network to adapt and evolve.

Water templated hydrogen-bonded network of pyridine amide appended carbamate in solid state

Ghosh, Kumaresh,Adhikari, Suman,Fr?hlich, Roland

, p. 63 - 67 (2006)

The pyridine amide appended carbamates 1 and 2 have been synthesized and their hydrogen-bonded self-assemblies in solid state have been described. The self-association pattern is dependent on the nature the anchored group of the carbamate moiety and influ

Compositional Persistence in a Multicyclic Network of Synthetic Replicators

Huck, Jürgen,Kosikova, Tamara,Philp, Douglas

, p. 13905 - 13913 (2019/10/05)

The emergence of collections of simple chemical entities that create self-sustaining reaction networks, embedding replication and catalysis, is cited as a potential mechanism for the appearance on the early Earth of systems that satisfy minimal definitions of life. In this work, a functional reaction network that creates and maintains a set of privileged replicator structures through auto- and cross-catalyzed reaction cycles is created from the pairwise combinations of four reagents. We show that the addition of individual preformed templates to this network, representing instructions to synthesize a specific replicator, induces changes in the output composition of the system that represent a network-level response. Further, we establish through sets of serial transfer experiments that the catalytic connections that exist between the four replicators in this network and the system-level behavior thereby encoded impose limits on the compositional variability that can be induced by repeated exposure to instructional inputs, in the form of preformed templates, to the system. The origin of this persistence is traced through kinetic simulations to the properties and inter-relationships between the critical ternary complexes formed by the auto- and crosscatalytic templates. These results demonstrate that in an environment where there is no continuous selection pressure the network connectivity, described by the catalytic relationships and system-level interactions between the replicators, is persistent, thereby limiting the ability of this network to adapt and evolve.

Manipulating replication processes within a dynamic covalent framework

Del Amo, Vicente,Slawin, Alexandra M. Z.,Philp, Douglas

supporting information; experimental part, p. 4589 - 4592 (2009/05/07)

(Chemical Equation Presented) The reaction of an amine bearing an amidopyridine recognition site and an aldehyde bearing a carboxylic acid recognition site affords an imine that is capable of directing its own formation through a dynamic covalent replicat

Troger's base molecular scaffolds in dicarboxylic acid recognition

Goswami, Shyamaprosad,Ghosh, Kumaresh,Dasgupta, Swagata

, p. 1907 - 1914 (2007/10/03)

Artificial receptors (1-5) have been designed and synthesized from simple precursors. The chain length selectivity studies of dicarboxylic acids within the cavities of new fluorescent Troger's base molecular frameworks (1- 3) have been carried out with a critical examination of their role of rigidity as well as flexibility in selective binding in comparison to receptor 5. The chiral resolution of the racemic Troger's base receptors (1 and 2) by chiral recognition with (+)- camphoric acid using hydrogen-bonding interactions has been studied.

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