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887908-65-8

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887908-65-8 Usage

General Description

The chemical (4-Diethoxymethyl-[1,2,3]triazol-1-yl)-acetic acid ethyl ester is an organic compound that contains triazole and acetic acid functional groups. It is commonly used as a building block in organic synthesis and medicinal chemistry. This chemical is also known for its potential biological activities, particularly in the development of pharmaceutical drugs. As an ethyl ester, it has improved solubility and can be readily utilized in various organic reactions. Its structure and properties make it a valuable tool for creating novel molecules with potential pharmacological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 887908-65-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,9,0 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 887908-65:
(8*8)+(7*8)+(6*7)+(5*9)+(4*0)+(3*8)+(2*6)+(1*5)=248
248 % 10 = 8
So 887908-65-8 is a valid CAS Registry Number.

887908-65-8Downstream Products

887908-65-8Relevant articles and documents

Copper(II) SBA-15: A reusable catalyst for azide-alkyne cycloaddition

Jlalia, Ibtissem,Gallier, Florian,Brodie-Linder, Nancy,Uziel, Jacques,Augé, Jacques,Lubin-Germain, Nadège

, p. 56 - 61 (2014/07/08)

The azide-alkyne cycloaddition reaction was investigated under catalytic conditions involving a copper(II) loaded silica based mesoporous material. Cu(II) SBA-15 demonstrated a high catalytic effect in 1,4-triazoles synthesis in organic. No additives such

Reusable polymer-supported catalyst for the [3+2] Huisgen cycloaddition in automation protocols

Girard, Christian,Oenen, Esra,Aufort, Marie,Beauviere, Sophie,Samson, Edmond,Herscovici, Jean

, p. 1689 - 1692 (2007/10/03)

A polymer-supported catalyst for Huisgen's [3+2] cycloaddition reaction between azides and alkynes was prepared from copper(I) iodide and Amberlyst A-21. This catalyst was then used in an automated synthesis of 1,4-disubstituted 1,2,3-triazoles giving acc

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