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28298-26-2

3,4-Dichloro-N-(2-hydroxyethyl)benzenecarboxamide, a chemical compound with the molecular formula C9H10Cl2NO2, is a derivative of benzenecarboxamide featuring two chlorine atoms and a hydroxyethyl group attached to the benzene ring. 3,4-DICHLORO-N-(2-HYDROXYETHYL)BENZENECARBOXAMIDE is recognized for its potential in pharmaceutical and agrochemical applications due to its antiviral and anticancer properties, positioning it as a promising candidate for drug development. It also serves as a valuable reagent in chemical research and synthesis.

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  • 28298-26-2 Structure

  • Basic information

    1. Product Name: 3,4-DICHLORO-N-(2-HYDROXYETHYL)BENZENECARBOXAMIDE
    2. Synonyms: 3,4-DICHLORO-N-(2-HYDROXYETHYL)BENZENECARBOXAMIDE;3,4-Dichloro-N-(2-hydroxyethyl)benzamide
    3. CAS NO:28298-26-2
    4. Molecular Formula: C9H9Cl2NO2
    5. Molecular Weight: 234.07926
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 28298-26-2.mol

  • Chemical Properties

    1. Melting Point: 153-155
    2. Boiling Point: 388.5 °C at 760 mmHg
    3. Flash Point: 188.8 °C
    4. Appearance: /
    5. Density: 1.395 g/cm3
    6. Vapor Pressure: 9.89E-07mmHg at 25°C
    7. Refractive Index: 1.58
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3,4-DICHLORO-N-(2-HYDROXYETHYL)BENZENECARBOXAMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3,4-DICHLORO-N-(2-HYDROXYETHYL)BENZENECARBOXAMIDE(28298-26-2)
    12. EPA Substance Registry System: 3,4-DICHLORO-N-(2-HYDROXYETHYL)BENZENECARBOXAMIDE(28298-26-2)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 28298-26-2(Hazardous Substances Data)

28298-26-2 Usage

Uses

Used in Pharmaceutical Industry:
3,4-DICHLORO-N-(2-HYDROXYETHYL)BENZENECARBOXAMIDE is used as an active pharmaceutical ingredient for its antiviral and anticancer properties, contributing to the development of new drugs that target a range of diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 3,4-DICHLORO-N-(2-HYDROXYETHYL)BENZENECARBOXAMIDE is utilized as a key component in the formulation of products designed to protect crops from viral infections and other threats, thereby enhancing agricultural productivity.
Used in Chemical Research and Synthesis:
3,4-DICHLORO-N-(2-HYDROXYETHYL)BENZENECARBOXAMIDE is employed as a reagent in chemical research, facilitating the synthesis of various compounds and contributing to the advancement of scientific knowledge in the field of chemistry.
It is crucial to handle 3,4-DICHLORO-N-(2-HYDROXYETHYL)BENZENECARBOXAMIDE with appropriate safety measures to mitigate any potential hazards associated with its use.

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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