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ETHYL 1-(4,6-DICHLORO-1,3,5-TRIAZIN-2-YL)PIPERIDINE-4-CARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

216502-45-3

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216502-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 216502-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,5,0 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 216502-45:
(8*2)+(7*1)+(6*6)+(5*5)+(4*0)+(3*2)+(2*4)+(1*5)=103
103 % 10 = 3
So 216502-45-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H14Cl2N4O2/c1-2-19-8(18)7-3-5-17(6-4-7)11-15-9(12)14-10(13)16-11/h7H,2-6H2,1H3

216502-45-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 1-(4,6-DICHLORO-1,3,5-TRIAZIN-2-YL)PIPERIDINE-4-CARBOXYLATE

1.2 Other means of identification

Product number -
Other names ethyl 1-(4,6-dichloro-1,3,5-triazin-2-yl)-4-piperidinecarboxylate

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:216502-45-3 SDS

216502-45-3Downstream Products

216502-45-3Relevant academic research and scientific papers

Synthesis and PI 3-kinase inhibition activity of some novel 2,4,6-trisubstituted 1,3,5-triazines

Nelson, Ronald A,Schronce, Taylor,Huang, Yue,Albugami, Alanoud,Kulik, George,Welker, Mark E.

, (2018)

A number of new trisubstituted triazine phosphatidylinositol 3-kinase (PI3K) inhibitors were prepared via a three-step procedure utilizing sequential nucleophilic aromatic substitution and cross-coupling reactions. All were screened as PI3K inhibitors relative to the well-characterized PI3K inhibitor, ZSTK474. The most active inhibitors prepared here were 2–4 times more potent than ZSTK474. A leucine linker was attached to the most active inhibitor since it would remain on any peptide-containing prodrug after cleavage by a prostate-specific antigen, and it did not prevent inhibition of protein kinase B (Akt) phosphorylation, and hence, the inhibition of PI3K by the modified inhibitor.

NOVEL SEH INHIBITORS AND THEIR USE

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Page/Page column 60-61, (2009/05/28)

The invention is directed to novel sEH inhibitors and their use in the treatment of diseases mediated by the sEH enzyme. Specifically, the invention is directed to compounds according to Formula I: (I) wherein R1, R2, R3, R5a, R6a A, B, Y, x, and m are defined below, and to pharmaceutically-acceptable salts thereof. The compounds of the invention are sEH inhibitors and can be used in the treatment of diseases mediated by the sEH enzyme, such as hypertension. Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting sEH and treatment of conditions associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.

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