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228107-17-3

2-Amino-4-phenylnaphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 228107-17-3 Structure

  • Basic information

    1. Product Name: 2-Amino-4-phenylnaphthalene
    2. Synonyms: 2-Amino-4-phenylnaphthalene;3-aMino-1-phenylnaphthalene
    3. CAS NO:228107-17-3
    4. Molecular Formula: C16H13N
    5. Molecular Weight: 219.28112
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 228107-17-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Amino-4-phenylnaphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Amino-4-phenylnaphthalene(228107-17-3)
    11. EPA Substance Registry System: 2-Amino-4-phenylnaphthalene(228107-17-3)

  • 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: 228107-17-3(Hazardous Substances Data)

228107-17-3 Usage

Properties

Pale yellow solid at room temperature

Structure

Naphthalene core with an amino group and phenyl group attached at the 2 and 4 positions of the naphthalene ring

Uses

Precursor in synthesis of pharmaceuticals and dyes, potential applications in organic electronics and as a molecular probe in biological research

Safety precautions

Due to aromatic structure and potential health hazards, handle with caution and in accordance with proper safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 228107-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,1,0 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 228107-17:
(8*2)+(7*2)+(6*8)+(5*1)+(4*0)+(3*7)+(2*1)+(1*7)=113
113 % 10 = 3
So 228107-17-3 is a valid CAS Registry Number.

228107-17-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenylnaphthalen-2-amine

1.2 Other means of identification

Product number -
Other names 3-amino-1-phenylnaphthalene

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:228107-17-3 SDS

228107-17-3Downstream Products

228107-17-3Relevant articles and documents

Aromaticity-Dependent Regioselectivity in Pd(II)-Catalyzed C-H Direct Arylation of Aryl Ureas

Jiang, Pingping,Li, Feng,Xu, Yongbao,Liu, Qingwen,Wang, Jing,Ding, Hong,Yu, Renfu,Wang, Qifeng

, p. 5918 - 5921 (2015)

Palladium-catalyzed C-H direct arylation generally occurs on the ortho-position of directing groups. By comparing meta-arylated products of 2-naphthyl urea to ortho-arylated products of phenyl urea, the ortho- and meta-regioselectivity of aryl ureas were found to depend on the aromaticity of the corresponding aryl substituents. Thus, aromaticity is a new factor which can affect the regioselectivity in C-H direct arylation. The finding was further confirmed by regioselective direct arylation of indole and pyrrole derivatives.

Asymmetric pyrene derivatives comprising amine group including heteroaryl group and naphthyl group and organic light-emitting diode including the same

-

Paragraph 0198; 0207-0210, (2021/02/02)

The present invention relates to a pyrene derivative represented by [chemical formula A] or [chemical formula B], and an organic light emitting diode comprising the same, wherein substituents Py_1, Py_2, Naph_1, and Naph_2, and m are as defined in the detailed description of the invention.

Novel potent and selective central 5-HT3 receptor ligands provided with different intrinsic efficacy. 2. Molecular basis of the intrinsic efficacy of arylpiperazine derivatives at the central 5-HT3 receptors

Cappelli, Andrea,Anzini, Maurizio,Vomero, Salvatore,Canullo, Laura,Mennuni, Laura,Makovec, Francesco,Doucet, Edith,Hamon, Michel,Menziani, M. Cristina,De Benedetti, Pier G.,Bruni, Giancarlo,Romeo, Maria R.,Giorgi, Gianluca,Donati, Alessandro

, p. 1556 - 1575 (2007/10/03)

Novel 5-HT3 receptor ligands were designed and synthesized with the aim of obtaining deeper insight into the molecular basis of the intrinsic efficacy of arylpiperazines interacting with the central 5-HT3 receptor. The newly synthesi

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