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High quality purity >99% 3,4,5-trihydroxybenzoyl chloride 35388-10-4 for sale We supply high quality 3,4,5-trihydroxybenzoyl chloride (CAS 35388-10-4), in stock, factory directly supply to clients, lower prices, more competitiveness.
What is the 3,4,5-trihydroxybenzoyl chloride ?
3,4,5-trihydroxybenzoyl chloride is , while it's Molecular Formula is C7H5 Cl O4. Used in Chemical Synthesis:
3,4,5-Trihydroxybenzoyl chloride is used as a reagent in chemical synthesis for the creation of complex molecules. Its aromatic properties and the presence of hydroxyl groups make it a versatile building block in the synthesis of various organic compounds.
Used in Scientific Research:
In the field of scientific research, 3,4,5-trihydroxybenzoyl chloride serves as a valuable tool for studying the properties and reactions of benzoic acid derivatives. It aids in understanding the behavior of aromatic compounds and their potential applications in different chemical processes.
While the practical applications of 3,4,5-trihydroxybenzoyl chloride outside of scientific research are currently limited, its role in chemical synthesis and research is significant. Further exploration and development may reveal additional uses for 3,4,5-trihydroxybenzoyl chloride in various industries.
What is the CAS number for 3,4,5-trihydroxybenzoyl chloride ?
The CAS number of 3,4,5-trihydroxybenzoyl chloride is 35388-10-4.
More information of 3,4,5-trihydroxybenzoyl chloride 35388-10-4 are:
|
Synonyms |
3,4,5-Trihydroxybenzoylchloride; Galloyl chloride |
|
CAS?Number |
35388-10-4 |
|
Molecular Formula |
C7H5 Cl O4 |
|
Molecular Weight |
188.567 |
|
Density |
1.696g/cm3 |
|
Boiling Point |
441.1°Cat760mmHg |
|
Flash Point |
220.6°C |
|
PSA |
77.76000 |
|
LogP |
1.18240 |
What is 3,4,5-trihydroxybenzoyl chloride (35388-10-4) used for?
3,4,5-Trihydroxybenzoyl chloride, also known as Galloyl Chloride, is a chemical compound that belongs to the family of benzoic acid and derivatives. It has the molecular formula C7H5ClO4 and features a benzene ring with three hydroxyl groups attached, which imparts it with aromatic properties. Despite its potential applications in chemical synthesis, exposure to it may cause eye irritation, and it can be harmful if ingested. Its uses are primarily in scientific research and as a reagent or building block for synthesizing more complex molecules.
InChI:InChI=1/C7H5ClO4/c8-7(12)3-1-4(9)6(11)5(10)2-3/h1-2,9-11H
Articles related to 3,4,5-trihydroxybenzoyl chloride:
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Article |
Source |
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Photorelease of a metal-binding pharmacophore from a Ru(ii) polypyridine complex |
Karges, Johannes,Stokes, Ryjul W.,Cohen, Seth M. supporting information, p. 2757 - 2765 (2021/03/09) |
|
Synthesis of hyperbranched glycodendrimers incorporating α-thiosialosides based on a gallic acid core |
Meunier, Serge J.,Wu, Quigquan,Wang, Sho-Nong,Roy, Rene , p. 1472 - 1482 (2007/10/03) |
How to get the best price on 3,4,5-trihydroxybenzoyl chloride?
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