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CAS

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122987-01-3

N-(4-chlorophenyl)-2,6-difluoro-, with the molecular formula C6H3ClF2, is a fluoroarene derivative of phenyl. It features a chlorine atom attached to the fourth carbon and two fluorine atoms on the second and sixth carbons. As an aromatic compound, it possesses unique properties and reactivity due to the presence of chloro and difluoro groups, which may influence its applications in chemical synthesis, pharmaceuticals, and agrochemicals.

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  • 122987-01-3 Structure

  • Basic information

    1. Product Name: N-(4-chlorophenyl)-2,6-difluoro-
    2. Synonyms: N-(4-chlorophenyl)-2,6-difluoro-;N-(2,6-Difluorobenzoyl)-4-chloroaniline;N-(4-Chlorophenyl)-2,6-difluorobenzaMide;Benzamide, N-(4-chlorophenyl)-2,6-difluoro
    3. CAS NO:122987-01-3
    4. Molecular Formula: C13H8ClF2NO
    5. Molecular Weight: 267.6585264
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122987-01-3.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.: Room Temperature, under inert atmosphere
    8. Solubility: Chloroform (Slightly), Methanol (Slightly)
    9. CAS DataBase Reference: N-(4-chlorophenyl)-2,6-difluoro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-chlorophenyl)-2,6-difluoro-(122987-01-3)
    11. EPA Substance Registry System: N-(4-chlorophenyl)-2,6-difluoro-(122987-01-3)

  • 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: 122987-01-3(Hazardous Substances Data)

122987-01-3 Usage

Uses

Used in Chemical Synthesis:
N-(4-chlorophenyl)-2,6-difluorois used as a building block in chemical synthesis for creating various organic compounds. Its unique structure allows for versatile reactions and the formation of new molecules with potential applications in different industries.
Used in Pharmaceuticals:
In the pharmaceutical industry, N-(4-chlorophenyl)-2,6-difluorois used as an intermediate or a key component in the development of new drugs. Its specific properties and reactivity can contribute to the synthesis of pharmaceutical compounds with desired therapeutic effects.
Used in Agrochemicals:
N-(4-chlorophenyl)-2,6-difluorois utilized in the agrochemical sector for the synthesis of pesticides, herbicides, and other crop protection agents. Its unique structure and reactivity can lead to the development of more effective and targeted agrochemicals.
Further research and experimentation are necessary to fully understand the potential uses and effects of N-(4-chlorophenyl)-2,6-difluoroin these industries and explore its full potential.

Check Digit Verification of cas no

The CAS Registry Mumber 122987-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,9,8 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 122987-01:
(8*1)+(7*2)+(6*2)+(5*9)+(4*8)+(3*7)+(2*0)+(1*1)=133
133 % 10 = 3
So 122987-01-3 is a valid CAS Registry Number.

122987-01-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-Chlorophenyl)-2,6-difluorobenzamide

1.2 Other means of identification

Product number -
Other names N-(2,6-difluorobenzoyl)-4-chloroaniline

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:122987-01-3 SDS

122987-01-3Downstream Products

122987-01-3Relevant articles and documents

Synthesis of 2-aminophenols and heterocycles by Ru-catalyzed C-H mono- and dihydroxylation

Yang, Xinglin,Shan, Gang,Rao, Yu

supporting information, p. 2334 - 2337 (2013/07/04)

A novel and efficient synthesis of 2-aminophenols, 2-aminobenzene-1,3- diols, and heterocycles through Ru-catalyzed C-H mono- and dihydroxylation of anilides has been developed with a new directing group strategy. The reaction demonstrates excellent reactivity, regioselectivity, good functional group tolerance, and high yields.

KINETICS OF METHANOLYSIS OF 1-(2-HALOGENO AND 2,6-DIHALOGENOBENZOYL)-3-(4-CHLOROPHENYL)UREAS

Kavalek, Jaromir,Kacetl, Lubomir,Kavalkova, Marcela

, p. 1363 - 1369 (2007/10/02)

The methanolysis kinetics has been measured of 1-(2,6-difluorobenzoyl)-3-(4-chlorophenyl)urea (a larvicidal insecticide Dimilin) and of four other mono- and dihalogenobenzoyl derivatives.Polar and steric effects of halogen on the rate and dissociation constants is discussed.

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