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3-Methoxy-2-(tributylstannyl)pyridine is a chemical compound characterized by a pyridine ring with a methoxy group and a tributylstannyl group attached to it. 3-Methoxy-2-(tributylstannyl)pyridine is notable for its role in organic synthesis, where it serves as a reagent for the introduction of the tributylstannyl group into organic molecules. The tributylstannyl group is particularly significant in organometallic chemistry due to its ability to be easily converted into other functional groups, rendering 3-Methoxy-2-(tributylstannyl)pyridine a versatile building block for the synthesis of complex organic molecules. Furthermore, the methoxy group in the molecule acts as a directing group in certain chemical reactions, facilitating selective functionalization of the pyridine ring. As such, 3-Methoxy-2-(tributylstannyl)pyridine is a valuable asset in the synthetic chemist's toolkit for constructing a wide array of organic molecules.

1094072-15-7

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1094072-15-7 Usage

Uses

Used in Organic Synthesis:
3-Methoxy-2-(tributylstannyl)pyridine is used as a reagent for the introduction of the tributylstannyl group into organic molecules, which is crucial for the synthesis of complex organic compounds. The tributylstannyl group's ability to be easily converted into other functional groups makes 3-Methoxy-2-(tributylstannyl)pyridine a key component in the creation of diverse organic molecules.
Used in Organometallic Chemistry:
In organometallic chemistry, 3-Methoxy-2-(tributylstannyl)pyridine is utilized for its tributylstannyl group, which is significant for its conversion into various functional groups. This property is essential for the development of new organometallic compounds and materials.
Used in Selective Functionalization:
3-Methoxy-2-(tributylstannyl)pyridine is used as a directing group in certain chemical reactions, allowing for the selective functionalization of the pyridine ring. This selective approach is vital for the precise synthesis of target molecules with specific desired properties.
Used in Pharmaceutical and Agrochemical Industries:
3-Methoxy-2-(tributylstannyl)pyridine is employed as a building block in the synthesis of pharmaceuticals and agrochemicals, where its ability to introduce the tributylstannyl group and facilitate selective functionalization contributes to the development of new drugs and pesticides with improved efficacy and selectivity.
Used in Material Science:
In material science, 3-Methoxy-2-(tributylstannyl)pyridine is used in the synthesis of new materials with unique properties, such as conductive polymers, sensors, and other advanced materials, leveraging its role in organometallic chemistry and its ability to be selectively functionalized.

Check Digit Verification of cas no

The CAS Registry Mumber 1094072-15-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,4,0,7 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1094072-15:
(9*1)+(8*0)+(7*9)+(6*4)+(5*0)+(4*7)+(3*2)+(2*1)+(1*5)=137
137 % 10 = 7
So 1094072-15-7 is a valid CAS Registry Number.

1094072-15-7 Well-known Company Product Price

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  • Aldrich

  • (SYX00048)  3-Methoxy-2-(tributylstannyl)pyridine  AldrichCPR

  • 1094072-15-7

  • SYX00048-1G

  • 2,901.60CNY

  • Detail

1094072-15-7SDS

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 tributyl-(3-methoxypyridin-2-yl)stannane

1.2 Other means of identification

Product number -
Other names 3-Methoxy-2-(tributylstannyl)pyridine

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:1094072-15-7 SDS

1094072-15-7Downstream Products

1094072-15-7Relevant academic research and scientific papers

Synthesis of 2-(2-Pyridyl)-2 H-azirines via Metal-Free C-C Cross-Coupling of Bromoazirines with 2-Stannylpyridines

Agafonova, Anastasiya V.,Smetanin, Ilia A.,Rostovskii, Nikolai V.,Khlebnikov, Alexander F.,Novikov, Mikhail S.

supporting information, p. 8045 - 8049 (2021/10/20)

A high-yield method for the introduction of a 2-pyridyl substituent in the C2 position of the three-membered ring of 2-bromo-2H-azirine-2-carboxylic acid derivatives by the direct cross-coupling with 2-(trialkylstannyl)pyridines has been described. The reaction works well with 3-, 4-, or 5-substituted 2-stannylpyridines and can be also employed for the synthesis of 2-(thiazol-2-yl)-2H-azirines. According to DFT calculations, the reaction proceeds through the sequence of SN2′-substitution of bromine, 1,4-stannyl shift, and [2,3]-sigmatropic shift of the pyridine ring.

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