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(Z,Z)-1-(4-Bromophenyl)-3,4-dihydroxy-6-(4-methylphenyl)-2,4-hexadiene-1,6-dione is a conjugated diketone compound characterized by its unique structure, featuring two hydroxy groups and two phenyl groups attached to a hexadiene chain. The (Z,Z) designation denotes the specific relative stereochemistry of the double bonds within the molecule, which contributes to its potential reactivity and applications in various scientific fields.

139266-58-3

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139266-58-3 Usage

Uses

Used in Organic Synthesis:
(Z,Z)-1-(4-Bromophenyl)-3,4-dihydroxy-6-(4-methylphenyl)-2,4-hexadiene-1,6-dione is used as a key intermediate in organic synthesis for the development of novel compounds with tailored properties. Its conjugated system and reactivity make it a promising candidate for creating new molecules with potential applications in various industries.
Used in Materials Science:
In the field of materials science, (Z,Z)-1-(4-Bromophenyl)-3,4-dihydroxy-6-(4-methylphenyl)-2,4-hexadiene-1,6-dione is used as a building block for designing materials with specific characteristics. The presence of the bromophenyl and 4-methylphenyl groups allows for the creation of materials with tailored properties, such as improved stability, conductivity, or optical properties.
Used in Medicinal Chemistry Research:
(Z,Z)-1-(4-Bromophenyl)-3,4-dihydroxy-6-(4-methylphenyl)-2,4-hexadiene-1,6-dione is used as a starting compound in medicinal chemistry research. Its potential biological activity and the possibility of specific interactions with biological targets make it an interesting candidate for the development of new drugs or drug candidates.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (Z,Z)-1-(4-Bromophenyl)-3,4-dihydroxy-6-(4-methylphenyl)-2,4-hexadiene-1,6-dione is used as a precursor for the synthesis of new drugs. Its unique structure and potential reactivity offer opportunities for the development of innovative therapeutic agents with improved efficacy and selectivity.
Used in Chemical Research and Development:
(Z,Z)-1-(4-Bromophenyl)-3,4-dihydroxy-6-(4-methylphenyl)-2,4-hexadiene-1,6-dione is used as a research compound in chemical research and development. Its conjugated system and the presence of functional groups make it an attractive molecule for studying various chemical reactions and exploring its potential applications in different fields of science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 139266-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,2,6 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 139266-58:
(8*1)+(7*3)+(6*9)+(5*2)+(4*6)+(3*6)+(2*5)+(1*8)=153
153 % 10 = 3
So 139266-58-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H15BrO4/c1-12-2-4-13(5-3-12)16(21)10-18(23)19(24)11-17(22)14-6-8-15(20)9-7-14/h2-11,21-22H,1H3/b16-10-,17-11-

139266-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-bromophenyl)-1,6-dihydroxy-6-(4-methylphenyl)hexa-1,5-diene-3,4-dione

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:139266-58-3 SDS

139266-58-3Downstream Products

139266-58-3Relevant academic research and scientific papers

1,3,4,6-Tetracarbonyl compounds. 3. Synthesis, structural features, and antimicrobial activity of 1,6-diaryl-3,4-dihydroxy-2,4-hexadiene-1,6-diones

Igidov,Koz'minykh,Sof'ina,Shironina,Koz'minykh

, p. 1276 - 1285 (2007/10/03)

The Wittig reaction of 5-aryl-2,3-dihydro-2,3-furandiones with aroylmethylenetriphenylphosphoranes is regioselective and leads to the formation of 5-aryl-2-aroylmethylene-2,3-dihydro-3-furanones. In the presence of acid the products react with water, givi

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