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2,6-Dichloro-3-nitroacetophenone, a derivative of acetophenone, is a yellow crystalline solid with the chemical formula C8H5Cl2NO3. It features a phenyl ring with two chlorine atoms and a nitro group attached, making it a versatile intermediate in the synthesis of various organic compounds.

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  • 223785-76-0 Structure
  • Basic information

    1. Product Name: 2,6-Dichloro-3-nitroacetophenone
    2. Synonyms: 2,6-Dichloro-3-nitroacetophenone;1-(2,6-dichloro-3-nitrophenyl)ethanone
    3. CAS NO:223785-76-0
    4. Molecular Formula: C8H5Cl2NO3
    5. Molecular Weight: 234.0362
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 223785-76-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,6-Dichloro-3-nitroacetophenone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,6-Dichloro-3-nitroacetophenone(223785-76-0)
    11. EPA Substance Registry System: 2,6-Dichloro-3-nitroacetophenone(223785-76-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 223785-76-0(Hazardous Substances Data)

223785-76-0 Usage

Uses

Used in Pharmaceutical Industry:
2,6-Dichloro-3-nitroacetophenone is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into the molecular structures of various drugs, contributing to their therapeutic properties.
Used in Dye Industry:
In the dye industry, 2,6-Dichloro-3-nitroacetophenone is utilized as a precursor in the production of dyes, where its chemical structure plays a role in determining the color and properties of the final dye products.
Used in Agrochemical Industry:
2,6-Dichloro-3-nitroacetophenone serves as an intermediate in the synthesis of agrochemicals, specifically in the creation of pesticides and other chemical products used in agriculture to protect crops and enhance yields.
Used as a Reagent in Organic Chemistry:
2,6-Dichloro-3-nitroacetophenone is also employed as a reagent in various organic chemistry reactions, facilitating important transformations and syntheses in the laboratory setting.
Safety Note:
It is crucial to handle 2,6-Dichloro-3-nitroacetophenone with care due to its toxic nature and potential to cause irritation to the skin, eyes, and respiratory system. Proper safety measures should be taken to minimize exposure and ensure the well-being of individuals working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 223785-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,7,8 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 223785-76:
(8*2)+(7*2)+(6*3)+(5*7)+(4*8)+(3*5)+(2*7)+(1*6)=150
150 % 10 = 0
So 223785-76-0 is a valid CAS Registry Number.

223785-76-0SDS

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 1-(2,6-Dichloro-3-nitrophenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2',6'-DICHLORO-3'-NITROACETOPHENONE

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:223785-76-0 SDS

223785-76-0Upstream product

223785-76-0Relevant articles and documents

Synthesis anti-HIV-1 activity of 4,5,6,7-tetrahydro-5-methylimidazo[4,5,1- jk][1,4]benzodiazepin-2(1H)-one (TIBO) derivatives. 3

Breslin,Kukla,Ludovici,Mohrbacher,Ho,Miranda,Rodgers,Hitchens,Leo,Gauthier,Ho,Scott,De Clercq,Pauwels,Andries,Janssen,Janssen

, p. 771 - 793 (2007/10/02)

4,5,6,7-Tetrahydro-5-methylimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-ones (TIBO), 1, have been shown to significantly inhibit HIV-1 replication in vitro by interfering with the virus's reverse transcriptase enzyme. They have also demonstrated potential cl

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