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2-Chloro-4-fluoro-benzamidine, a member of the benzamidine class, is a white crystalline solid characterized by its molecular formula C7H6ClFN2 and a molecular weight of 170.59 g/mol. It is recognized for its versatility as a building block in organic synthesis, particularly in the creation of pharmaceuticals and agrochemicals.

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  • 582306-90-9 Structure
  • Basic information

    1. Product Name: 2-CHLORO-4-FLUORO-BENZAMIDINE
    2. Synonyms: 2-CHLORO-4-FLUORO-BENZAMIDINE
    3. CAS NO:582306-90-9
    4. Molecular Formula: C7H6ClFN2
    5. Molecular Weight: 172.59
    6. EINECS: N/A
    7. Product Categories: pharmacetical
    8. Mol File: 582306-90-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 275.3°C at 760 mmHg
    3. Flash Point: 120.3°C
    4. Appearance: /
    5. Density: N/A
    6. Vapor Pressure: 0.00396mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-CHLORO-4-FLUORO-BENZAMIDINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-CHLORO-4-FLUORO-BENZAMIDINE(582306-90-9)
    12. EPA Substance Registry System: 2-CHLORO-4-FLUORO-BENZAMIDINE(582306-90-9)
  • 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: 582306-90-9(Hazardous Substances Data)

582306-90-9 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-4-fluoro-benzamidine is utilized as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of compounds with specific biological activities, making it a valuable asset in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chloro-4-fluoro-benzamidine serves as a crucial component in the synthesis of pesticides and other crop protection agents. Its incorporation into these products enhances their effectiveness in controlling pests and diseases, thereby supporting agricultural productivity and food security.
Used as a Reagent:
2-Chloro-4-fluoro-benzamidine also functions as a reagent in the preparation of biologically active compounds. Its ability to participate in various chemical reactions facilitates the synthesis of a broad spectrum of molecules with potential applications in research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 582306-90-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,2,3,0 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 582306-90:
(8*5)+(7*8)+(6*2)+(5*3)+(4*0)+(3*6)+(2*9)+(1*0)=159
159 % 10 = 9
So 582306-90-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClFN2.ClH/c8-6-3-4(9)1-2-5(6)7(10)11;/h1-3H,(H3,10,11);1H

582306-90-9SDS

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 2-chloro-4-fluorobenzenecarboximidamide

1.2 Other means of identification

Product number -
Other names 2-Chloro-4-fluorobenzimidamide

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:582306-90-9 SDS

582306-90-9Downstream Products

582306-90-9Relevant articles and documents

INHINITORS OF GLI1 AS THERAPEUTIC AGENTS

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Paragraph 0183, (2020/06/10)

This disclosure relates to compounds, pharmaceutical compositions comprising them, and methods of using the compounds and compositions for treating diseases related to glioma- associated oncogene (Gli) expression. More particularly, this disclosure relate

Pyridine and pyrimidine derivatives

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, (2008/06/13)

The present invention provides compounds of formula (I) wherein R1, R2, R3, R4 and X are as defined in the specification, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment

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