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CAS

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10569-67-2

[1,1':2',1''-Terphenyl]-4'-amine is a specialty chemical compound characterized by its unique structure of three connected phenyl rings with a substituted amine group (-NH2) at the 4' position. This aromatic amine exhibits typical traits of aromatic amines, such as its potential to act as a base in chemical reactions. Its specific applications, toxicity, environmental impact, and potential uses are subject to in-depth research and may vary accordingly.

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  • 10569-67-2 Structure

  • Basic information

    1. Product Name: [1,1':2',1''-Terphenyl]-4'-amine
    2. Synonyms: [o-Terphenyl]-4'-amine(7CI,8CI); NSC 506444
    3. CAS NO:10569-67-2
    4. Molecular Formula: C18H15 N
    5. Molecular Weight: 245.324
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10569-67-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 387.5°Cat760mmHg
    3. Flash Point: 198.1°C
    4. Appearance: N/A
    5. Density: 1.103g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: [1,1':2',1''-Terphenyl]-4'-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: [1,1':2',1''-Terphenyl]-4'-amine(10569-67-2)
    11. EPA Substance Registry System: [1,1':2',1''-Terphenyl]-4'-amine(10569-67-2)

  • 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: 10569-67-2(Hazardous Substances Data)

10569-67-2 Usage

Uses

Used in Research Applications:
[1,1':2',1''-Terphenyl]-4'-amine is used as a building block for more complex polymers in research settings, contributing to the development of novel materials and compounds.
Used in Industrial Applications:
In the industry, [1,1':2',1''-Terphenyl]-4'-amine is utilized as a heat transfer agent, leveraging its thermal properties to facilitate efficient heat exchange processes in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 10569-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,6 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10569-67:
(7*1)+(6*0)+(5*5)+(4*6)+(3*9)+(2*6)+(1*7)=102
102 % 10 = 2
So 10569-67-2 is a valid CAS Registry Number.

10569-67-2SDS

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 3,4-diphenylaniline

1.2 Other means of identification

Product number -
Other names [1,1':2',1''-Terphenyl]-4'-amine

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:10569-67-2 SDS

10569-67-2Relevant articles and documents

Acid-Catalyzed Reactions of N-Arylhydroxylamines and Related Compounds with Benzene. Iminium-Benzenium Ions

Shudo, Koichi,Ohta, Toshiharu,Okamoto, Toshihiko

, p. 645 - 653 (2007/10/02)

N-Arylhydroxylamines react with benzene in the presence of trifluoroacetic acid (TFA) at room temperature to give diphenylamines.When TFA was replaced by a strong acid, trifluoromethanesulfonic acid (TFSA), the major products were aminobiphenyls.The nature of the reaction was explored by reactions of 4-substituted phenylhydroxylamines and dialkylaniline N-oxides with benzene.Thus, it was demonstrated that the reactive intermediates are onium-benzenium dications which are trapped by benzene to give aminobiphenyls by a mechanism similar to the Friedel-Krafts alkylation.Further evidence for the proposed reaction mechanism was the observation that nitrosobenzene and azoxybenzene reacted with benzene to give analogous products in the presence of the stronger acid.

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