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1,7,8-trifluoronaphthalen-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

676545-61-2

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676545-61-2 Usage

Derivative of

Naphthalene

Attached atoms

Three fluorine atoms and one hydroxyl group

Usage

a. Organic synthesis
b. Building block for pharmaceuticals and agrochemicals
c. Intermediate in production of dyes and fluorescent materials

Physical state

White solid

Melting point

High

Solubility

Low in water

Applications

Various uses in the chemical industry

Check Digit Verification of cas no

The CAS Registry Mumber 676545-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,5,4 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 676545-61:
(8*6)+(7*7)+(6*6)+(5*5)+(4*4)+(3*5)+(2*6)+(1*1)=202
202 % 10 = 2
So 676545-61-2 is a valid CAS Registry Number.

676545-61-2SDS

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 1,7,8-trifluoronaphthalen-2-ol

1.2 Other means of identification

Product number -
Other names 1,7,8-trifluoro-2-naphthol

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:676545-61-2 SDS

676545-61-2Downstream Products

676545-61-2Relevant academic research and scientific papers

Facile synthesis of 1,7,8-trifluoro-2-naphthol via DMAP catalyzed cycloaromatization

Araki, Keisuke,Katagiri, Tomohiro,Inoue, Munenori

, p. 41 - 47 (2014)

A facile synthesis of 1,7,8-trifluoro-2-naphthol, an important synthetic intermediate for liquid crystal compounds with a 1,7,8-trifluoronaphthalene structure, was developed starting from 4-bromo-1,2-difluorobenzene via DMAP catalyzed intramolecular cycloaromatization in 51% overall yield for the 6 steps.

Unilaterally Fluorinated Acenes: Synthesis and Solid-State Properties

Bischof, Daniel,Breuer, Tobias,Grell, Yvonne,Hofmann, Philipp E.,Ivlev, Sergei I.,Koert, Ulrich,Schiller, Anna L. C.,Tripp, Matthias W.,Witte, Gregor

, p. 16501 - 16505 (2020/07/20)

The rapid development of organic electronics is closely related to the availability of molecular materials with specific electronic properties. Here, we introduce a novel synthetic route enabling a unilateral functionalization of acenes along their long side, which is demonstrated by the synthesis of 1,2,10,11,12,14-hexafluoropentacene (1) and the related 1,2,9,10,11-pentafluorotetracene (2). Quantum chemical DFT calculations in combination with optical and X-ray absorption spectroscopy data indicate that the single-molecule properties of 1 are a connecting link between the organic semiconductor model systems pentacene (PEN) and perfluoropentacene (PFP). In contrast, the crystal structure analysis reveals a different packing motif than for the parent molecules. This can be related to distinct F???H interactions identified in the corresponding Hirshfeld surface analysis and also affects solid-state properties such as the exciton binding energy and the sublimation enthalpy.

1,7,8-TRIFLUORONAPHTHALENE-2-NAPHTHOL, AND METHOD FOR PRODUCING LIQUID CRYSTAL COMPOUND USING SAME

-

Page/Page column 10, (2010/02/12)

The present invention provides 1,7,8-trifluoro-2-naphthol and a derivative thereof as intermediates for efficiently producing a trifluoronaphthalene liquid crystal material. A method for efficiently producing a trifluoronaphthalene liquid crystal material

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