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963-46-2

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963-46-2 Usage

Common Use

Plasticizer in industrial applications

Physical State

Clear, colorless liquid

Solubility

Insoluble in water

Boiling Point

High boiling point

Function

Makes plastics more flexible and durable

Common Products

Vinyl flooring, wire and cable insulation, automotive parts

Safety Precautions

Handle with caution, may be harmful if swallowed, inhaled, or absorbed through the skin

Environmental Impact

May have detrimental effects on the environment if released into the air, water, or soil

Check Digit Verification of cas no

The CAS Registry Mumber 963-46-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 963-46:
(5*9)+(4*6)+(3*3)+(2*4)+(1*6)=92
92 % 10 = 2
So 963-46-2 is a valid CAS Registry Number.

963-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2,3,5,6-tetrafluoroterephthalate

1.2 Other means of identification

Product number -
Other names Tetrafluorterephthalsaeure-diethylester

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:963-46-2 SDS

963-46-2Relevant articles and documents

New preparation method of 1-bromo-methyl-2,3,5,6-tetrafluoro-4-(trifluoromethyl)benzene

-

Paragraph 0053-0054, (2019/08/20)

The invention discloses a new preparation method of 1-bromo-methyl-2,3,5,6-tetrafluoro-4-(trifluoromethyl)benzene. The method comprises the steps that with a compound 2,3,5,6-tetrafluoro-terephthalicacid as a raw material, through alkylation, 2,3,5,6-tetrafluoro-terephthalic acid diester is obtained firstly, then single hydrolysis is conducted, formic acid is fluorinated into trifluoromethyl so as to obtain 2,3,5,6-tetrafluoro-4-trifluoromethyl benzoate, and after the 2,3,5,6-tetrafluoro-4-trifluoromethyl benzoate is reduced into alcohol, through bromination, the target compound is obtained.According to the method, the reaction raw materials are easy to obtain and low in price, few reaction by-products are generated, and the product is easy to purify, high in yield and suitable for massindustrial production; therefore, reliable guarantee is provided for a key intermediate of a novel drug 2-hydroxyl-5-(2,3,5,6-tetrafluoro-4-trifluoromethyl benzylamino)benzoic acid.

Trifluoro-3-hydroxy-1H-indazolecarboxylic acids and esters from perfluorinated benzenedicarboxylic acids

Medina, Carlos Perez,Lopez, Concepcion,Claramunt, Rosa M.,Elguero, Jose

scheme or table, p. 890 - 899 (2010/04/23)

Twelve new 3-hydroxyindazoles, each bearing three fluorine substituents and a CO2R group (R = H, CH3, C2H5) distributed around its 4-, 5-, 6-, and 7-positions, have been synthesized. They were studied by NMR in

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