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4-Chloro-2,6-di(piperidin-1-yl)pyrimidine is a chemical compound with the molecular formula C16H24ClN5. It is a white crystalline solid that belongs to the class of pyrimidines, which are heterocyclic aromatic organic compounds containing two nitrogen atoms at positions 1 and 3 of a six-membered ring. This specific compound features a 4-chloro substituent and two piperidin-1-yl groups attached to the 2 and 6 positions of the pyrimidine core. The piperidin-1-yl groups are derived from piperidine, a cyclic amine with a six-membered ring structure. The presence of these substituents contributes to the compound's unique chemical properties and potential applications in various fields, such as pharmaceuticals and materials science.

4193-59-3

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4193-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4193-59-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,9 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4193-59:
(6*4)+(5*1)+(4*9)+(3*3)+(2*5)+(1*9)=93
93 % 10 = 3
So 4193-59-3 is a valid CAS Registry Number.

4193-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-2,6-di(piperidin-1-yl)pyrimidine

1.2 Other means of identification

Product number -
Other names pyrimidine,4-chloro-2,6-di-1-piperidinyl

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:4193-59-3 SDS

4193-59-3Downstream Products

4193-59-3Relevant academic research and scientific papers

Facile aromatic nucleophilic substitution (SNAr) reactions in ionic liquids: An electrophile-nucleophile dual activation by [Omim]Br for the reaction

Zhang, Xiao,Lu, Guo-Ping,Cai, Chun

, p. 5580 - 5585 (2016/10/21)

A facile aromatic nucleophilic substitution (SNAr) reaction in recyclable [Omim]Br under relatively mild conditions has been described. An electrophile-nucleophile dual activation by [Omim]Br is also discovered based on control experiments, 1H NMR and IR spectroscopies. This chemistry provides an efficient and metal-free approach for the generation of Caryl-X (XS, N, O) bonds, many of which are significant synthetic intermediates or drugs, making this methodology attractive to both synthetic and medicinal chemistry.

TRIAMINOPYRIMIDINE DERIVATIVES AS INHIBITORS OF CDC25 PHOSPHATASE

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Page/Page column 21, (2010/06/16)

The present invention relates to the novel triaminopyrimidine derivatives of formula (I) in which R1, R2, W, R3, R4, and R5 are variable groups. These products have a Cdc25-phosphatase-inhibiting activity. The invention also relates to a process for synth

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