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1,3-Benzenediol, 4-[4,6-bis(4-fluorophenyl)-1,3,5-triazin-2-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

804548-29-6

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804548-29-6 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. Derivative of 1,3-benzenediol (resorcinol)

Explanation

1,3-Benzenediol, 4-[4,6-bis(4-fluorophenyl)-1,3,5-triazin-2-yl]is derived from the parent compound 1,3-benzenediol, which is also known as resorcinol.
3. Contains four fluorophenyl groups

Explanation

The compound has four fluorine-containing phenyl groups attached to its structure, which contribute to its unique properties.
4. Contains a 1,3,5-triazin-2-yl group

Explanation

The compound also features a 1,3,5-triazin-2-yl group, which is a six-membered heterocyclic ring containing three nitrogen atoms.
5. Used in pharmaceuticals, agrochemicals, and materials science

Explanation

Due to its unique properties, the compound is utilized in the development and production of various products in different industries, such as pharmaceuticals, agrochemicals, and materials science.
6. Unique chemical and physical properties

Explanation

The compound possesses specific chemical and physical properties that make it suitable for a wide range of applications in the chemical industry.
7. Valuable intermediate compound for synthesis

Explanation

Its structure and properties make it an important intermediate compound for the synthesis of other complex organic molecules, which can be used in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 804548-29-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,4,5,4 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 804548-29:
(8*8)+(7*0)+(6*4)+(5*5)+(4*4)+(3*8)+(2*2)+(1*9)=166
166 % 10 = 6
So 804548-29-6 is a valid CAS Registry Number.

804548-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[4,6-bis(4-fluorophenyl)-1H-1,3,5-triazin-2-ylidene]-3-hydroxycyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 2,4-bis(4-fluorophenyl)-6-resorcinyl-1,3,5-triazine

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:804548-29-6 SDS

804548-29-6Relevant academic research and scientific papers

Polymerizable UV absorbers for the UV stabilization of polyesters. I. Design, synthesis and polymerization of a library of UV absorbing monomers

Cormack, Peter A.G.,Erdemli, Omer C.,Sankey, Stephen W.

, (2021/10/14)

UV stabilizers, such as Tinuvin 1577, are organic additives that are used in the polymer industry to suppress polymer photodegradation, however leaching of the stabilizers from polymers is a significant practical issue which limits the effectiveness of the stabilizers and restricts polymer lifetimes. Novel, polymerizable UV stabilizers were synthesised and copolymerized with bis(2-hydroxyethyl) isophthalate to yield poly(ethylene isophthalate) copolymers where the UV stabilizers are bound covalently into the polymer chains. This strategy prevents leaching of stabilizers from polymers over time, and is expected to lead to enhanced UV protection of polymers compared to the admixing of polymers with UV stabilizers of low molar mass.

AMINOARYL TRIAZINES

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Page 97-98, (2010/02/09)

A novel process for preparing a aminophenyltriazines of the formula (I’), comprises reacting a corresponding halogenophenyltriazine of the formula (I’’), with an amine of the formula (IX), H-NR'2R'3, wherein X is chloro or preferably

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