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4,5-Difluoro-2-nitrobenzonitrile is a chemical compound characterized by its molecular formula C7H2F2N2O2. It is a yellow solid that is highly reactive due to the presence of both nitro and cyano groups. This versatile reactivity, along with its unique structural properties, makes it a valuable building block in the field of organic chemistry.

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  • 165671-05-6 Structure
  • Basic information

    1. Product Name: 4,5-Difluoro-2-nitrobenzonitrile
    2. Synonyms: 3,4-Difluoro-6-nitrobenzonitrile;4,5-Difluoro-2-nitrobenzonitrile
    3. CAS NO:165671-05-6
    4. Molecular Formula: C7H2F2N2O2
    5. Molecular Weight: 184.1
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 165671-05-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 312.9°C at 760 mmHg
    3. Flash Point: 143°C
    4. Appearance: /
    5. Density: 1.51g/cm3
    6. Vapor Pressure: 0.000514mmHg at 25°C
    7. Refractive Index: 1.529
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4,5-Difluoro-2-nitrobenzonitrile(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4,5-Difluoro-2-nitrobenzonitrile(165671-05-6)
    12. EPA Substance Registry System: 4,5-Difluoro-2-nitrobenzonitrile(165671-05-6)
  • 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: 165671-05-6(Hazardous Substances Data)

165671-05-6 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
4,5-Difluoro-2-nitrobenzonitrile is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its reactivity allows for the preparation of a wide range of organic compounds, making it a crucial component in these industries.
Used in Dye and Pigment Production:
4,5-Difluoro-2-nitrobenzonitrile is also used as a reagent in the production of various dyes and pigments. Its unique properties contribute to the development of colorants with specific characteristics for different applications.
Used in Polymer and Specialty Chemical Manufacturing:
4,5-Difluoro-2-nitrobenzonitrile finds application in the manufacturing of polymers and other specialty chemicals. Its role in these processes is significant, as it helps in creating materials with tailored properties for specific uses.

Check Digit Verification of cas no

The CAS Registry Mumber 165671-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,6,7 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 165671-05:
(8*1)+(7*6)+(6*5)+(5*6)+(4*7)+(3*1)+(2*0)+(1*5)=146
146 % 10 = 6
So 165671-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H2F2N2O2/c8-5-1-4(3-10)7(11(12)13)2-6(5)9/h1-2H

165671-05-6SDS

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 4,5-difluoro-2-nitrobenzonitrile

1.2 Other means of identification

Product number -
Other names X4765

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:165671-05-6 SDS

165671-05-6Relevant articles and documents

HETEROCYCLIC INHIBITORS OF HISTAMINE RECEPTORS FOR THE TREATMENT OF DISEASE

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, (2011/10/05)

The present invention relates to compounds and methods which may be useful as inhibitors of H1R and/or H4R for the treatment or prevention of inflammatory, autoimmune, allergic, and ocular diseases.

Method for the production of N-(5-amino-2-cyano-4-fluoro-phenyl)-sulphonamides and new intermediate products

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, (2008/06/13)

The invention relates to a process for preparing N-(5-amino-2-cyano-4-fluoro-phenyl)-sulphonamides in which, in a first step, 2-amino-4,5-difluoro-benzonitrile is reacted with sulphonyl halides in the presence of an acid acceptor and in the presence of a

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