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74744-72-2

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74744-72-2 Usage

General Description

Diethyl 2-hydroxybenzene-1,4-dicarboxylate is a chemical compound with the molecular formula C14H18O5. It is commonly known as diethyl gentisate and is an ester derivative of gentisic acid. The compound is a white to pale yellow solid at room temperature and is insoluble in water but soluble in organic solvents. Diethyl gentisate is used in the manufacturing of pharmaceuticals and cosmetic products, and also has applications in the production of specialty chemicals. It is known for its antioxidant properties and is used in the development of antioxidant formulations. Additionally, the compound exhibits potential anti-inflammatory and analgesic properties, making it a compound of interest in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 74744-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,4 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74744-72:
(7*7)+(6*4)+(5*7)+(4*4)+(3*4)+(2*7)+(1*2)=152
152 % 10 = 2
So 74744-72-2 is a valid CAS Registry Number.

74744-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-hydroxybenzene-1,4-dicarboxylate

1.2 Other means of identification

Product number -
Other names Diethyl 2-hydroxyterephthalate

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:74744-72-2 SDS

74744-72-2Relevant articles and documents

Design, synthesis and conformational analyses of bifacial benzamide based foldamers

Rodriguez-Marin, Silvia,Murphy, Natasha S.,Shepherd, Helena J.,Wilson, Andrew J.

, p. 104187 - 104192 (2015/12/30)

The design, synthesis and conformational analyses of novel backbones represents a key focus of research that underpins efforts to exploit foldamers (i) in a biological setting e.g. as inhibitors of protein-protein interactions (PPIs) and (ii) for the purp

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