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3366-65-2

2-Aminophenanthrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 3366-65-2 Structure

  • Basic information

    1. Product Name: 2-Aminophenanthrene
    2. Synonyms: 2-Phenanthrylamine;phenanthren-2-aMine;2-Phenanthrenamine
    3. CAS NO:3366-65-2
    4. Molecular Formula: C14H11N
    5. Molecular Weight: 193.26
    6. EINECS: 213-431-6
    7. Product Categories: N/A
    8. Mol File: 3366-65-2.mol

  • Chemical Properties

    1. Melting Point: 85°C
    2. Boiling Point: 319.47°C (rough estimate)
    3. Flash Point: 229 °C
    4. Appearance: /
    5. Density: 1.208
    6. Vapor Pressure: 4.52E-07mmHg at 25°C
    7. Refractive Index: 1.5850 (estimate)
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-Aminophenanthrene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Aminophenanthrene(3366-65-2)
    12. EPA Substance Registry System: 2-Aminophenanthrene(3366-65-2)

  • 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: 3366-65-2(Hazardous Substances Data)

3366-65-2 Usage

Safety Profile

Questionable carcinogen with experimental tumorigenic data.Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 3366-65-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3366-65:
(6*3)+(5*3)+(4*6)+(3*6)+(2*6)+(1*5)=92
92 % 10 = 2
So 3366-65-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H11N/c15-12-7-8-14-11(9-12)6-5-10-3-1-2-4-13(10)14/h1-9H,15H2

3366-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name phenanthren-2-amine

1.2 Other means of identification

Product number -
Other names 2-aminophenathrene

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:3366-65-2 SDS

3366-65-2Relevant articles and documents

Selective Carbon-Carbon Bond Amination with Redox-Active Aminating Reagents: A Direct Approach to Anilines?

Qiu, Xu,Wang, Yachong,Su, Lingyu,Jin, Rui,Song, Song,Qin, Qixue,Li, Junhua,Zong, Baoning,Jiao, Ning

supporting information, p. 3011 - 3016 (2021/09/13)

Amines are among the most fundamental motifs in chemical synthesis, and the introduction of amine building blocks via selective C—C bond cleavage allows the construction of nitrogen compounds from simple hydrocarbons through direct skeleton modification. Herein, we report a novel method for the preparation of anilines from alkylarenes via Schmidt-type rearrangement using redox-active amination reagents, which are easily prepared from hydroxylamine. Primary amines and secondary amines were prepared from corresponding alkylarenes or benzyl alcohols under mild conditions. Good compatibility and valuable applications of the transformation were also displayed.

COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENTS, ORGANIC ELECTROLUMINESCENT ELEMENT AND ELECTRONIC DEVICE

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Paragraph 0225; 0226, (2018/08/25)

A compound represented by formula (1) provides a high performance organic electroluminescence device and a novel material for realizing such an organic electroluminescence device: wherein R1 to R6, a to f, L1 to L3, and Ar are as defined in the description.

A push-pull 4a,4b-dihydrophenanthrene

Lewis,Kurth,Kalgutkar

, p. 1372 - 1373 (2007/10/03)

Irradiation of (Z)-3-cyano-3′-aminostilbene in the absence of oxygen yields a push-pull substituted dihydrophenanthrene with substantial quinoidal character as evidenced by the pronounced solvent dependence of its absorption spectrum.

Luminescence of N-Arylbenzamides in Low-Temperature Glasses

Lewis, Frederick D.,Liu, Weizhong

, p. 9678 - 9686 (2007/10/03)

The low-temperature luminescence of benzamide and six additional N-arylbenzamides has been investigated in a methyltetrahydrofuran glass. The luminescence of microcrystalline benzamide has also been studied. Assignments of the fluorescence and phosphoresc

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