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122509-29-9

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122509-29-9 Usage

Description

2,3,6-Tricarboethoxypyridine, a chemical compound with the molecular formula C13H15NO4, is a versatile reagent in organic synthesis, particularly for the preparation of pyridine derivatives. This clear, colorless liquid exhibits a slightly sweet odor and is soluble in organic solvents. Its utility extends to the production of pharmaceutical compounds and agrochemicals, and it is valued for its ability to form stable complexes with transition metal ions in coordination chemistry. However, due to its flammable nature and potential to cause irritation to the eyes and skin, careful handling is required.

Uses

Used in Organic Synthesis:
2,3,6-Tricarboethoxypyridine is used as a reagent in organic synthesis for the preparation of pyridine derivatives, which are important building blocks in the creation of various organic compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,3,6-Tricarboethoxypyridine is used as a building block for the production of pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemicals:
2,3,6-Tricarboethoxypyridine is utilized in the agrochemical industry as a component in the synthesis of agrochemicals, aiding in the development of pesticides and other agricultural chemicals.
Used in Coordination Chemistry:
In coordination chemistry, 2,3,6-Tricarboethoxypyridine is used for its ability to form stable complexes with transition metal ions, which is valuable for research and applications in materials science and catalysis.

Check Digit Verification of cas no

The CAS Registry Mumber 122509-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,5,0 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122509-29:
(8*1)+(7*2)+(6*2)+(5*5)+(4*0)+(3*9)+(2*2)+(1*9)=99
99 % 10 = 9
So 122509-29-9 is a valid CAS Registry Number.

122509-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl pyridine-2,3,6-tricarboxylate

1.2 Other means of identification

Product number -
Other names 2,3,6-Pyridinetricarboxylicacid,2,3,6-triethyl ester

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:122509-29-9 SDS

122509-29-9Downstream Products

122509-29-9Relevant articles and documents

Cp*RuCl-catalyzed [2 + 2 + 2] cycloadditions of α,ω- diynes with electron-deficient carbon-heteroatom multiple bonds leading to heterocycles

Yamamoto, Yoshihiko,Kinpara, Keisuke,Saigoku, Tomoaki,Takagishi, Hideyuki,Okuda, Satoshi,Nishiyama, Hisao,Itoh, Kenji

, p. 605 - 613 (2005)

In the presence of a catalytic amount of Cp*RuCl(cod), 1,6-diynes were allowed to react chemoand regioselectively with electron-deficient nitriles and heterocumulenes at 60-90°C to afford heterocyclic compounds. The mechanism of the ruthenium-catalyzed regioselective formations of bicyclic pyridines and pyridones were analyzed on the basis of density functional calculations. Cyclocotrimerizations of ethyl propiolate with ethyl cyanoformate or propyl isocyanate gave rise to two of the four possible pyridine or pyridone regioisomers.

Preparation and inverse-electron-demand diels-alder reaction of an electron-deficient heterocyclic azadiene: Triethyl 1,2,4-triazine-3,5,6-tricarboxylate and 2,3,6-tricarboethoxypyridine

Boger, Dale L.,Panek, James S.,Yasuda, Masami

, p. 142 - 142 (2017/05/20)

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