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3,5-Difluoro-4-iodoaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1542-34-3 Structure
  • Basic information

    1. Product Name: 3,5-Difluoro-4-iodoaniline
    2. Synonyms: BUTTPARK 120\07-59;3,5-DIFLUORO-4-IODOANILINE;3,5-Difluoro-4-iodoaniline 97%;3,5-Difluoro-4-iodoaniline97%;3,5-difluoro-4-iodobenzenamine
    3. CAS NO:1542-34-3
    4. Molecular Formula: C6H4F2IN
    5. Molecular Weight: 255
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1542-34-3.mol
  • Chemical Properties

    1. Melting Point: 112
    2. Boiling Point: 270.597 °C at 760 mmHg
    3. Flash Point: 117.453 °C
    4. Appearance: /
    5. Density: 2.087 g/cm3
    6. Vapor Pressure: 0.00678mmHg at 25°C
    7. Refractive Index: 1.628
    8. Storage Temp.: 2-8°C(protect from light)
    9. Solubility: N/A
    10. PKA: 1.77±0.10(Predicted)
    11. CAS DataBase Reference: 3,5-Difluoro-4-iodoaniline(CAS DataBase Reference)
    12. NIST Chemistry Reference: 3,5-Difluoro-4-iodoaniline(1542-34-3)
    13. EPA Substance Registry System: 3,5-Difluoro-4-iodoaniline(1542-34-3)
  • 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: 1542-34-3(Hazardous Substances Data)

1542-34-3 Usage

Uses

3,5-Difluoro-4-Iodoaniline is a useful research chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 1542-34-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,4 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1542-34:
(6*1)+(5*5)+(4*4)+(3*2)+(2*3)+(1*4)=63
63 % 10 = 3
So 1542-34-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H4F2IN/c7-4-1-3(10)2-5(8)6(4)9/h1-2H,10H2

1542-34-3SDS

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 3,5-Difluoro-4-Iodoaniline

1.2 Other means of identification

Product number -
Other names 3,5-Difluoro-4-iodoaniline

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:1542-34-3 SDS

1542-34-3Upstream product

1542-34-3Downstream Products

1542-34-3Relevant articles and documents

Chlorination of aniline and methyl carbanilate by N-chlorosuccinimide and synthesis of 1,3,5-trichlorobenzene

Davis, Matthew C.

experimental part, p. 1100 - 1108 (2009/09/08)

Aniline undergoes regioselective trichlorination by N-chlorosuccinimide (NCS) in acetonitrile in good yield. The product 2,4,6-trichoroaniline was converted into 1,3,5-trichlorobenzene by reduction of its diazonium salt. Reaction of the methyl carbamate of aniline with NCS gave only the 2,4-dichlorophenyl carbamate. Copyright Taylor & Francis Group, LLC.

Synthesis and thiolation of 1,3-difluoro-2,4,6-trihaloanilines and benzenes

Manka, Jason T.,Kaszynski, Piotr

, p. 39 - 43 (2007/10/03)

Three pentahaloanilines were prepared by stepwise halogenation of 3,5-difluoroaniline and were deaminated to form pentahalobenzenes. Alternatively, two pentahalobenzenes were obtained by lithiation followed by iodination of 1,3-difluoro-4,6-dihalobenzenes

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