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71648-28-7

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71648-28-7 Usage

General Description

Ethyl 2,2-diethoxyacetimidate is a chemical compound used in organic synthesis as a reagent for the preparation of esters and amides. It is derived from ethylamine and diethyl carbonate, and it contains two ethoxy groups attached to the imidate functional group. The compound is commonly used as a protecting group for sensitive carbonyl compounds, as well as a reactant in the formation of β-lactams and other nitrogen-containing heterocycles. Ethyl 2,2-diethoxyacetimidate is known for its mild reaction conditions and high selectivity, making it a valuable tool in synthetic chemistry for the preparation of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 71648-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,4 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71648-28:
(7*7)+(6*1)+(5*6)+(4*4)+(3*8)+(2*2)+(1*8)=137
137 % 10 = 7
So 71648-28-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NO3/c1-4-10-7(9)8(11-5-2)12-6-3/h8-9H,4-6H2,1-3H3/b9-7-

71648-28-7SDS

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 2,2-diethoxyethanimidate

1.2 Other means of identification

Product number -
Other names 2,2-Diaethoxy-acetimidsaeure-aethylester

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:71648-28-7 SDS

71648-28-7Relevant articles and documents

Synthesis, guest binding, and metal coordination of functionalized self-folding deep cavitands

Mettry, Magi,Moehlig, Melissa P.,Hooley, Richard J.

supporting information, p. 1497 - 1500 (2015/03/30)

A simple method to introduce donor functions to the upper rim of self-folding benzimidazole-based deep cavitands is described. The upper rim donors allow controlled noncovalent binding of suitably sized guest species via both self-complementary hydrogen bonding and space-filling interactions, and metal-mediated self-folding is possible if bidentate coordinators are incorporated.

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