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2-[2-(1-methylethyl)-4-phenyltetrahydro-2H-pyran-4-yl]ethanaminium is a complex organic compound with the molecular formula C19H27NO. It is a derivative of tetrahydro-2H-pyran, featuring a 4-phenyl group and a 1-methylethyl substituent. The compound has a quaternary ammonium group, which is formed by the addition of a proton to the nitrogen atom in the ethanaminium moiety. This chemical structure is significant in the field of organic chemistry, particularly in the synthesis of pharmaceuticals and other specialty chemicals. The compound's unique arrangement of atoms and functional groups may confer specific properties that are relevant to its potential applications, such as its reactivity, solubility, or biological activity.

5669-18-1

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5669-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5669-18-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5669-18:
(6*5)+(5*6)+(4*6)+(3*9)+(2*1)+(1*8)=121
121 % 10 = 1
So 5669-18-1 is a valid CAS Registry Number.

5669-18-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-phenyl-2-propan-2-yloxan-4-yl)ethylazanium

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5669-18-1 SDS

5669-18-1Relevant academic research and scientific papers

Studies in Decarboxylation. Part 16. Steric Inhibition of Resonance in a 1,5-Sigmatropic Reaction

al-Borno, Amal,Bigley, David B.

, p. 1311 - 1312 (2007/10/02)

The rates of gas-phase decarboxylation of some 3-phenyl-substituted but-3-enoic acids are best rationalized in terms of steric inhibition of resonance in the more sterically crowded members.

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