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  • 699016-40-5 Structure
  • Basic information

    1. Product Name: 2-FLUORO-4-IODOBENZALDEHYDE
    2. Synonyms: 2-Fluoro-4-iodobenzadehyde;3-Fluoro-4-formyliodobenzene
    3. CAS NO:699016-40-5
    4. Molecular Formula: C7H4FIO
    5. Molecular Weight: 250.01
    6. EINECS: N/A
    7. Product Categories: Adehydes, Acetals & Ketones;Fluorine Compounds;Iodine Compounds
    8. Mol File: 699016-40-5.mol
    9. Article Data: 2
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 259.9 °C at 760 mmHg
    3. Flash Point: 111 °C
    4. Appearance: /
    5. Density: 1.962 g/cm3
    6. Vapor Pressure: 0.0126mmHg at 25°C
    7. Refractive Index: 1.64
    8. Storage Temp.: Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-FLUORO-4-IODOBENZALDEHYDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-FLUORO-4-IODOBENZALDEHYDE(699016-40-5)
    12. EPA Substance Registry System: 2-FLUORO-4-IODOBENZALDEHYDE(699016-40-5)
  • 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: 699016-40-5(Hazardous Substances Data)

699016-40-5 Usage

Description

2-FLUORO-4-IODOBENZALDEHYDE is a chemical compound characterized by the molecular formula C7H4FIO and a molecular weight of 248.01 g/mol. It is a pale yellow to light brown solid at room temperature, featuring a benzene ring with a fluorine atom at the 2-position and an iodine atom at the 4-position, along with an aldehyde functional group. 2-FLUORO-4-IODOBENZALDEHYDE is known for its role as an intermediate in the synthesis of a variety of pharmaceuticals, agrochemicals, and organic compounds, highlighting its importance in organic synthesis and its versatility in multiple industrial applications.

Uses

Used in Pharmaceutical Industry:
2-FLUORO-4-IODOBENZALDEHYDE is used as an intermediate in the synthesis of drugs and other bioactive compounds, contributing to the development of new medications and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-FLUORO-4-IODOBENZALDEHYDE serves as a key intermediate in the production of various agrochemicals, potentially enhancing crop protection and management strategies.
Used in Organic Synthesis:
2-FLUORO-4-IODOBENZALDEHYDE is utilized as a versatile intermediate in organic synthesis, facilitating the creation of a wide range of organic compounds for diverse applications.
Used as a Reagent in Chemical Reactions:
2-FLUORO-4-IODOBENZALDEHYDE also functions as a reagent in multiple chemical reactions, further expanding its utility across various industries that rely on chemical processes for their products or operations.

Check Digit Verification of cas no

The CAS Registry Mumber 699016-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,9,0,1 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 699016-40:
(8*6)+(7*9)+(6*9)+(5*0)+(4*1)+(3*6)+(2*4)+(1*0)=195
195 % 10 = 5
So 699016-40-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H4FIO/c8-7-3-6(9)2-1-5(7)4-10/h1-4H

699016-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoro-4-iodobenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-Fluoro-4-formyliodobenzene

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:699016-40-5 SDS

699016-40-5Relevant articles and documents

SUBSTITUTED HYDANTOINS

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Page/Page column 10-11, (2009/07/17)

The present invention relates to compounds of the formula methods for the preparation thereof, and methods for their use. The compounds are useful in treating diseases characterized by the hyperactivity of MEK. Accordingly the compounds are useful in the treatment of diseases, such as cancer, cognitive and CNS disorders, and inflammatory/autoimmune diseases.

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