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The chemical compound "1-[3-[[3-[(3-acetyl-5-chloro-2-hydroxy-phenyl)methyl]-5-chloro-2-hydroxy-phenyl]methyl]-5-chloro-2-hydroxy-phenyl]ethanone" is a complex organic molecule with a molecular formula of C23H17Cl3O4. It features a central ethanone (keto) group, with three phenyl rings, each substituted with various functional groups. The phenyl rings are connected through methylene bridges, and the molecule contains three chlorine atoms and one acetyl group. 1-[3-[[3-[(3-acetyl-5-chloro-2-hydroxy-phenyl)methyl]-5-chloro-2-hydroxy-phenyl]methyl]-5-chloro-2-hydroxy-phenyl]ethanone is characterized by its unique structure, which includes multiple chloro and hydroxy substitutions on the phenyl rings, as well as an acetyl group attached to one of the phenyl rings. Due to its complexity, 1-[3-[[3-[(3-acetyl-5-chloro-2-hydroxy-phenyl)methyl]-5-chloro-2-hydroxy-phenyl]methyl]-5-chloro-2-hydroxy-phenyl]ethanone may have specific applications in chemical research or as an intermediate in the synthesis of other complex organic molecules.

6342-14-9

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6342-14-9 Usage

Explanation

The compound is composed of 22 carbon atoms, 16 hydrogen atoms, 6 chlorine atoms, and 4 oxygen atoms.

Explanation

The compound is a yellow-colored solid at room temperature.

Explanation

The chemical structure of the compound contains three aromatic rings.

Explanation

Each of the three aromatic rings in the compound contains chlorine and hydroxyl groups.

Explanation

The compound has an acetyl group (-COCH3) attached to one of its aromatic rings.

Explanation

The compound is commonly used as a starting material or intermediate in the synthesis of various pharmaceutical and agrochemical products.

Explanation

The compound serves as a valuable intermediate for the production of flavonoid compounds, which are important in the fields of medicine and biology.

Explanation

The compound's structure allows it to be used in the synthesis of other biologically active molecules.

Appearance

Yellow solid

Aromatic rings

Three

Chlorine and hydroxyl groups

Present in each aromatic ring

Acetyl group

Attached to one of the rings

Common use

Synthesis of pharmaceutical and agrochemical products

Intermediate for flavonoid compounds

Yes

Biologically active molecules

Can be used to produce

Check Digit Verification of cas no

The CAS Registry Mumber 6342-14-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6342-14:
(6*6)+(5*3)+(4*4)+(3*2)+(2*1)+(1*4)=79
79 % 10 = 9
So 6342-14-9 is a valid CAS Registry Number.

6342-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-[[3-[(3-acetyl-5-chloro-2-hydroxyphenyl)methyl]-5-chloro-2-hydroxyphenyl]methyl]-5-chloro-2-hydroxyphenyl]ethanone

1.2 Other means of identification

Product number -
Other names 1,1'-{(5-chloro-2-hydroxybenzene-1,3-diyl)bis[methanediyl(5-chloro-2-hydroxybenzene-3,1-diyl)]}diethanone

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:6342-14-9 SDS

6342-14-9Upstream product

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