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5-Iodo-3-methyl-2-pyridinamine is a chemical compound characterized by the molecular formula C6H6IN3. It is a pyridine derivative, featuring an iodine atom and a methyl group attached to the 3 and 2 positions of the pyridine ring, respectively. 5-Iodo-3-methyl-2-pyridinamine is known for its potential in the synthesis of pharmaceuticals and agrochemicals, and it holds promise in the realm of medicinal chemistry due to its unique chemical structure and properties. It serves as a valuable building block in the creation of novel drugs and agricultural chemicals, and its versatility extends to various industrial and research applications.

166266-19-9

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166266-19-9 Usage

Uses

Used in Pharmaceutical Synthesis:
5-Iodo-3-methyl-2-pyridinamine is utilized as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs. Its chemical structure allows for the creation of compounds with specific therapeutic properties, making it an essential component in medicinal chemistry.
Used in Agrochemical Synthesis:
In the agrochemical industry, 5-Iodo-3-methyl-2-pyridinamine is employed as a precursor in the production of various agricultural chemicals. Its incorporation into these products can enhance their effectiveness in pest control and crop protection, thereby contributing to increased agricultural productivity.
Used in Medicinal Chemistry Research:
5-Iodo-3-methyl-2-pyridinamine is also used as a research compound in medicinal chemistry. It aids scientists in understanding the structure-activity relationships of potential drug candidates and in the optimization of their pharmacological profiles.
Used in Industrial Applications:
Beyond its use in pharmaceuticals and agrochemicals, 5-Iodo-3-methyl-2-pyridinamine may find applications in other industries where its unique chemical properties can be leveraged for specific purposes, such as in the development of new materials or chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 166266-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,2,6 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 166266-19:
(8*1)+(7*6)+(6*6)+(5*2)+(4*6)+(3*6)+(2*1)+(1*9)=149
149 % 10 = 9
So 166266-19-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H7IN2/c1-4-2-5(7)3-9-6(4)8/h2-3H,1H3,(H2,8,9)/p+1

166266-19-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (H27510)  2-Amino-5-iodo-3-methylpyridine, 95%   

  • 166266-19-9

  • 250mg

  • 691.0CNY

  • Detail
  • Alfa Aesar

  • (H27510)  2-Amino-5-iodo-3-methylpyridine, 95%   

  • 166266-19-9

  • 1g

  • 1597.0CNY

  • Detail
  • Aldrich

  • (ADE000317)  5-Iodo-3-methyl-pyridin-2-ylamine  AldrichCPR

  • 166266-19-9

  • ADE000317-1G

  • 1,611.09CNY

  • Detail

166266-19-9SDS

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 5-Iodo-3-methyl-2-pyridinamine

1.2 Other means of identification

Product number -
Other names 5-iodo-3-methylpyridin-2-amine

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:166266-19-9 SDS

166266-19-9Relevant articles and documents

SULFONYL COMPOUNDS THAT INTERACT WITH GLUCOKINASE REGULATORY PROTEIN

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Page/Page column 213, (2013/08/28)

The present invention relates to sulfonyl compounds that interact with glucokinase regulatory protein. In addition, the present invention relates to methods of treating type 2 diabetes, and other diseases and/or conditions where glucokinase regulatory protein is involved using the compounds, or pharmaceutically acceptable salts thereof, and pharmaceutical compositions that contain the compounds, or pharmaceutically acceptable salts thereof.

Substituted 2H-1,3-benzoxazin-4(3H)-ones

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Page/Page column 23, (2010/10/20)

Substituted benzoxazin-4(3H)-ones are provided which are useful for treating thrombosis and for reducing the likelihood and/or severity of a secondary ischemic event in a patient.

Synthesis of a dA-dT base pair analogue and its effects on DNA-ligand binding

Lan, Tao,McLaughlin, Larry W.

, p. 198 - 210 (2007/10/03)

Two nucleoside derivatives containing the base analogues 3-deazaadenine and 3-methyl-2-pyridone have been prepared as analogues of dA and dT, respectively. After conversion into the appropriately protected phosphoramidites, DNA sequences were prepared with site-specifically placed analogues. When present in a duplex DNA sequence, the analogues result in the deletion of one or both of the hydrogen bonding functional groups (the N3-nitrogen of dA and the O2-carbonyl of dT) present in the minor groove. Binding by two ligands, 4′,6-diamidine-2-phenyl indole (DAPI) and Hoechst 33258 in the minor groove has been probed using a variety of DNA sequences. These sequences contain a d(GAATTC)2 core with analogue nucleosides substituted for one or more of the dA and dT residues. DAPI bound strongly to any sequence that contained both O2-carbonyls of the central two dT residues. The presence of a dc3A residue did in some cases enhance binding. With one of the central O2-carbonyls deleted, the binding was noticeably reduced, and with both absent, no significant binding could be detected. Similar although less dramatic results were observed with Hoechst 33258 binding to analogue sequences.

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