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4,6-Dimethyl-2-(3,4,5-trimethoxyphenyl)pyrimidine is a chemical compound characterized by its unique molecular structure. It features a pyrimidine ring, which is a six-membered heterocyclic aromatic organic compound with four carbon atoms and two nitrogen atoms. The compound is further distinguished by the presence of two methyl groups at the 4 and 6 positions on the pyrimidine ring, and a 3,4,5-trimethoxyphenyl group attached at the 2 position. The trimethoxyphenyl group consists of a benzene ring with three methoxy groups (-OCH3) attached at the 3, 4, and 5 positions. This specific arrangement of functional groups endows the compound with particular chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

4156-74-5

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4156-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4156-74-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,5 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4156-74:
(6*4)+(5*1)+(4*5)+(3*6)+(2*7)+(1*4)=85
85 % 10 = 5
So 4156-74-5 is a valid CAS Registry Number.

4156-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dimethyl-2-(3,4,5-trimethoxyphenyl)pyrimidine

1.2 Other means of identification

Product number -
Other names 4,6-dimethyl-2-(3,4,5-trimethoxy-phenyl)-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:4156-74-5 SDS

4156-74-5Relevant academic research and scientific papers

Self-Assembly of Non-Biological Polymeric Strands Undergoing Enforced Helical Self-Organization

Schmitt, Jean-Louis,Lehn, Jean-Marie

, p. 3417 - 3426 (2003)

The polycondensation of a dihydrazino-pyrimidine (5 and 6) with a pyrimidine-dicarbaldehyde (7 and 8b) provides an efficent access to helical polymeric strands based on the formation of hydrazone connections between the pyrimidine groups. The folding into a helical structure is enforced by the helicity codon defined by the (hydrazone-pyrimidine) sequence. The polymers obtained have been characterized by mass spectrometry, indicating molecular weights up to ca. 12000 Da. Electronic spectra display specific absorption and emission features. These helical polymers present a core diameter of ca. 20 A, a pitch of 3.5 A, and, for a molecular weight around 9000 Da, a height of ca. 42 A with 12 turns. The self-assembled helical polymers obtained represent stable frameworks for the lateral attachment of functional residues in a helical disposition. Such entities may possess a range of novel chemical as well as biological properties.

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