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28298-26-2

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28298-26-2 Usage

General Description

3,4-Dichloro-N-(2-hydroxyethyl)benzenecarboxamide is a chemical compound with the molecular formula C9H10Cl2NO2. It is a derivative of benzenecarboxamide, and it has two chlorine atoms and a hydroxyethyl group attached to the benzene ring. 3,4-DICHLORO-N-(2-HYDROXYETHYL)BENZENECARBOXAMIDE is commonly used in the production of pharmaceuticals and agrochemicals. It has been found to exhibit antiviral and anticancer properties, making it a potential candidate for drug development. Additionally, it is also used as a reagent in chemical research and synthesis. However, it is important to handle this compound with proper safety precautions, as it may be hazardous if mishandled.

Check Digit Verification of cas no

The CAS Registry Mumber 28298-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,9 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28298-26:
(7*2)+(6*8)+(5*2)+(4*9)+(3*8)+(2*2)+(1*6)=142
142 % 10 = 2
So 28298-26-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9Cl2NO2/c10-7-2-1-6(5-8(7)11)9(14)12-3-4-13/h1-2,5,13H,3-4H2,(H,12,14)

28298-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dichloro-N-(2-hydroxyethyl)benzamide

1.2 Other means of identification

Product number -
Other names 3,4-Dichlor-benzoesaeure-(2-hydroxy-ethylamid)

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:28298-26-2 SDS

28298-26-2Relevant articles and documents

Oxazolines. 3. Regioselective Synthesis of 2-(Monosubstituted phenyl) and/or Unsymmetrically 2-(Disubstituted phenyl) 2-Oxazolines by Cross-Coupling Grignard Reagents to (Haloaryl)-2-oxazolines

Pridgen, Lendon N.

, p. 4319 - 4323 (2007/10/02)

2-(Monosubstituted phenyl) 2-oxazoline 5 (R = H) and unsymmetrically 2-(disubstituted phenyl) 2-oxazolines 5 have been prepared by cross-coupling alkyl and aryl Grignard reagents to 2-(mono- and dihalogenated phenyl) 2-oxazolines 2 and 3 (X = halogen), re

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