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57871-18-8

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57871-18-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57871-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,7 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57871-18:
(7*5)+(6*7)+(5*8)+(4*7)+(3*1)+(2*1)+(1*8)=158
158 % 10 = 8
So 57871-18-8 is a valid CAS Registry Number.

57871-18-8SDS

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 methyl pyrimidine-2-carboximidate

1.2 Other means of identification

Product number -
Other names methyl ester of imino-pyrimidine acid

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:57871-18-8 SDS

57871-18-8Relevant articles and documents

A self-assembled, magnetically coupled square Cu16 4 x [2 x 2] grid

Dawe, Louise N.,Thompson, Laurence K.

, p. 7440 - 7444 (2007)

(Chemical Equation Presented) Grid ion: A Cu16 grid prepared with a tetratopic bishydrazone ligand has metal ions in a [4 x 4] array linked by a combination of μ-Ohydrazone and μ-NNpyridazine bridges. The six-coordinate copper ions display Jahn-Teller distortion, leading to some orbitally orthogonal bridges. Multiple intragrid magnetic-exchange pathways are present and are modeled simply by taking the molecular symmetry and the orthogonal connections into account.

Synthesis of three imidazole derivatives and corrosion inhibition performance for copper

He, Kang,Hou, Yanggao,Lei, Jiaheng,Ma, Sicai,Yang, Ze,Zhu, Limeng

, (2022/01/26)

Three imidazole derivatives, including 3-(4-(2,4-dichlorophenyl)-5-methyl-1H-imidazol-2-yl)pyridine (PDI), 2-(4-(2,4-dichlorophenyl)-5-methyl-1H-imidazol-2-yl)pyrazine (PAI) and 2-(4-(2,4-dichlorophenyl)-5-methyl-1H-imidazol-2-yl)pyrimidine (PMI), were synthesized. The structure of these compounds was confirmed by LC-MS, 1H NMR, 13C NMR and FTIR spectra. The inhibition performance in 3.5 wt% NaCl was investigated by electrochemical measurement and surface analysis. Results show that the corrosion efficiency of PDI (95.93%) was higher than PAI (69.61%) and PMI (20.46%), which is consistent with the adsorption energy calculated by molecular dynamics simulation. The corrosion inhibition mechanism could be explained by the metal–organic polymer film formed on the copper surface: on the one hand, the π-system formed by aromatic rings is tightly adsorbed on the copper substrates; on the other hand, the nitrogen atoms in the imidazole ring are coordinated with the metal ions in solution to form metal–organic polymer which could improve the compactness of the hydrophobic film.

A one-pot approach to 10-(1H-1,2,3-triazol-1-yl)pyrimido[1,2-a]indoles via aryne-mediated transformations of 3-(pyrimidin-2-yl)-1,2,4-triazines

Kopchuk, Dmitry S.,Chepchugov, Nikolay V.,Khasanov, Albert F.,Kovalev, Igor S.,Santra, Sougata,Nosova, Emiliya V.,Zyryanov, Grigory V.,Majee, Adinath,Rusinov, Vladimir L.,Chupakhin, Oleg N.

supporting information, p. 3862 - 3865 (2016/08/02)

An efficient synthetic approach toward 10-(1H-1,2,3-triazol-1-yl)pyrimido[1,2-a]indoles, including fluorinated derivatives, has been developed. The transformation of the 1,2,4-triazine ring of readily available 3-(pyrimidin-2-yl)-1,2,4-triazines proceeds

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