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Pyrimidine, 4-(4-pyridinyl)(9CI) is a heterocyclic aromatic organic compound with the molecular formula C9H7N3. It belongs to the pyrimidine family and features a pyrimidine ring with an attached pyridinyl group at position 4. This unique structure and reactivity make it a valuable intermediate for various organic synthesis reactions.

53345-78-1

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53345-78-1 Usage

Uses

Used in Pharmaceutical Industry:
Pyrimidine, 4-(4-pyridinyl)(9CI) is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agricultural Industry:
Pyrimidine, 4-(4-pyridinyl)(9CI) is also used as a precursor in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products to improve crop yield and protection.

Check Digit Verification of cas no

The CAS Registry Mumber 53345-78-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,4 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53345-78:
(7*5)+(6*3)+(5*3)+(4*4)+(3*5)+(2*7)+(1*8)=121
121 % 10 = 1
So 53345-78-1 is a valid CAS Registry Number.

53345-78-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-pyridin-4-ylpyrimidine

1.2 Other means of identification

Product number -
Other names 4-(4-pyridyl)pyrimidine

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:53345-78-1 SDS

53345-78-1Downstream Products

53345-78-1Relevant academic research and scientific papers

PYRIDINIUM COMPOUNDS AND THEIR USE AS HERBICIDES

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Page/Page column 67, (2020/08/28)

Compounds of the formula (I) wherein the substituents are as defined in claim 1, useful as a pesticides, especially as herbicides.

HERBICIDAL PYRIDINIUM COMPOUNDS

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Page/Page column 66-67, (2020/08/22)

Compounds of the formula (I) wherein the substituents are as defined in claim 1, useful as a pesticides, especially as herbicides.

Indolizines and pyrrolo[1,2-c]pyrimidines decorated with a pyrimidine and a pyridine unit respectively

Popa, Marcel Mirel,Georgescu, Emilian,Caira, Mino R.,Georgescu, Florentina,Draghici, Constantin,Stan, Raluca,Deleanu, Calin,Dumitrascu, Florea

, p. 1079 - 1088 (2015/08/18)

The three possible structural isomers of 4-(pyridyl)pyrimidine were employed for the synthesis of new pyrrolo[1,2-c]pyrimidines and new indolizines, by 1,3-dipolar cycloaddition reaction of their corresponding N-ylides generated in situ from their corresp

One-pot and three-component synthesis of substituted pyrimidines catalysed by boron sulfuric acid under solvent-free conditions

Soheilizad, Mehdi,Adiba, Mehdi,Sajjadifarb, Sami

, p. 524 - 527 (2014/12/10)

An efficient, simple and one-pot synthesis of pyrimidine derivatives by a three-component reaction of ketones, triethyl orthoformate, and ammonium acetate in the presence of boron sulfuric acid as a reusable and efficient catalyst under solvent-free conditions is reported. The reusability of catalyst, simplicity of the starting materials, short reaction time, one-pot, and good yields of products are the main advantages.

One-pot synthesis of pyrimidines under solvent-free conditions

Ghorbani-Vaghei, Ramin,Karimi-Nami, Rahman,Toghraei-Semiromi, Zahra,Amiri, Mostafa,Salimi, Zahra,Ghavidel, Mehdi

, p. 324 - 330 (2014/04/17)

N,N,N',N'-Tetrabromobenzene-1,3-disulfonamide was used as an efficient catalyst for the one-pot synthesis of pyrimidine derivatives in excellent yields from triethoxymethane, ammonium acetate, and various ketone derivatives at 100-110 °C under solvent-fre

Novel synthesis of bihetaryl compounds

Nishiwaki, Nagatoshi,Yamashita, Keiko,Azuma, Mayumi,Adachi, Tomoko,Tamura, Mina,Ariga, Masahiro

, p. 1996 - 2000 (2007/10/03)

The ring transformation of nitropyrimidinone 1 with acetophenone derivatives 2 affords two kinds of azaheterocyclic compounds, 4-phenylpyrimidines 3 and 3-nitro-6-phenyl-2-pyridones 4. On the basis of the relationship between electronic properties of the substituent and ratios of products, a plausible reaction mechanism is provided. Furthermore, the present reaction could be applied to heterocyclic ketones giving bihetaryl compounds.

Photochemical ring contraction of 4-heteroaryl-substituted 1,4(or 3,4)-dihydropyrimidines into imidazoles

Stoel, R. E. van der,Plas, H. C. van der,Jongejan, H.

, p. 364 - 367 (2007/10/02)

Photolysis of 4-R-1,4(or 3,4)-dihydropyrimidines causes ring contraction into imidazoles, provided that the substituent R is capable of sufficiently stabilizing an anionic centre (R=2-thiazolyl, 2-pyridyl, 4-pyridyl).Chemical evidence is presented to show

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