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4,6-DIMETHYL-2-(4-METHOXYPHENYL)PYRIMIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154499-87-3

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154499-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154499-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,4,9 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 154499-87:
(8*1)+(7*5)+(6*4)+(5*4)+(4*9)+(3*9)+(2*8)+(1*7)=173
173 % 10 = 3
So 154499-87-3 is a valid CAS Registry Number.

154499-87-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-bis-methyl-2-(4'-methoxyphenyl)pyrimidine

1.2 Other means of identification

Product number -
Other names 2-(p-methoxyphenyl)-4,6-dimethylpyrimidine

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:154499-87-3 SDS

154499-87-3Relevant academic research and scientific papers

Transition-Metal-Free Cross-Coupling of Aryl and Heteroaryl Thiols with Arylzinc Reagents

Yang, Bo,Wang, Zhong-Xia

, p. 6220 - 6223 (2017/11/24)

Cross-coupling of (hetero)arylthiols with arylzinc reagents via C-S cleavage was performed under transition-metal-free conditions. The reaction displays a wide scope of substrates and high functional-group tolerance. Electron-rich and -deficient (hetero)arylthiols and arylzinc reagents can be employed in this transformation. Mg2+ and Li+ ions were demonstrated to facilitate the reaction.

An expeditious route toward pyrazine-containing nucleoside analogues

Modha, Sachin G.,Trivedi, Jalpa C.,Mehta, Vaibhav P.,Ermolat'ev, Denis S.,Van Der Eyckens, Erik V.

supporting information; experimental part, p. 846 - 856 (2011/04/17)

An improved and convenient methodology for the synthesis of asymmetrically substituted pyrazines starting from 3,5-dichloropyrazin-2(1H)-ones has been elaborated. Several nucleoside analogues have been synthesized containing the pyrazine core as the organic base coupled with the sugar via a triazole linkage. The beneficial effect of microwave irradiation throughout the sequence has been demonstrated.

Molecular motion in zinc hydrazone grid complexes

Dutta, Manisha,Movassat, Meisam,Brook, David J.R.,Oliver, Allen,Ward, Don

experimental part, p. 632 - 643 (2012/03/27)

Four new grid forming hydrazone ligands substituted with methoxy and dimethylamino groups were synthesised. Combination of these ligands with zinc triflate in acetonitrile resulted in self-assembly to form grids as indicated by 1H NMR and ES-MS

A convenient method for the preparation of highly substituted 1101 pyrimidines: Synthesis of tri- and tetra-subsituted pyrimidines from 1,3-dicarbonyl compounds and N,N,N′-tris-(trimethylsilyl)amidines

Ghosh, Usha,Katzenellenbogen, John A.

, p. 1101 - 1104 (2007/10/03)

A modification of the Pinner pyrimidine synthesis has been developed that utilizes trimethylsilyl amidines and results in greatly improved yield of highly substituted pyrimidines.

SYNTHESIS OF PYRIMIDINYL TRIFLATES AND PALLADIUM-CATALYZED COUPLING WITH ORGANOTIN AND ORGANOZINC REAGENTS

Sandosham, Jessie,Undheim, Kjell

, p. 501 - 514 (2007/10/02)

Pyrimidinyl triflates have been synthesized from pyrimidinones using triflic anhydride in the presence of triethylamine.The triflates, in the pyrimidine electrophilic positions, are versatile intermediates for substitution reactions.Carbon substituents ar

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