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Phenol, 4-(2-hydroxyethoxy)-2-methoxy-, also known as 2-methoxy-4-(2-hydroxyethoxy)phenol, is an organic compound with the chemical formula C9H12O4. It is a derivative of phenol, featuring a hydroxyethoxy group at the 4-position and a methoxy group at the 2-position. Phenol, 4-(2-hydroxyethoxy)-2-methoxy- is characterized by its ability to form hydrogen bonds due to the presence of hydroxyl groups, which can influence its solubility and reactivity. It is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and other organic compounds. The compound's structure allows for potential interactions with enzymes and receptors, making it a candidate for biological activity studies.

3556-03-4

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3556-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3556-03-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,5 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3556-03:
(6*3)+(5*5)+(4*5)+(3*6)+(2*0)+(1*3)=84
84 % 10 = 4
So 3556-03-4 is a valid CAS Registry Number.

3556-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-hydroxyethoxy)-2-methoxyphenol

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

1.5 Emergency phone number

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More Details:3556-03-4 SDS

3556-03-4Relevant academic research and scientific papers

PRODRUGS OF OXAZOLIDINONE CETP INHIBITORS

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Page/Page column 14, (2010/04/27)

The compounds of Formula I are prodrugs of CETP inhibitors having a central oxazolidinone ring. The compounds cyclize by the elimination of HX to form an oxazolidinone ring after administration to a patient.

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