29654-55-5 Usage
Description
3,5-Dihydroxybenzyl alcohol is a white to light yellow crystal powder that serves as a versatile building block and monomer in the synthesis of various dendritic polyether macromolecules and dendrimers.
Uses
Used in Dendrimers and Polymer Synthesis:
3,5-Dihydroxybenzyl alcohol is used as a dendrimer building block for the creation of complex and highly branched structures with potential applications in various fields, such as drug delivery, nanotechnology, and materials science.
Used in the Synthesis of Dendritic Polyether Macromolecules:
3,5-Dihydroxybenzyl alcohol is used as a monomer for the synthesis of a series of monodisperse dendritic polyether macromolecules, which can be further functionalized and utilized in various applications.
Used in Dimethylsilyl Linked Dendrimers:
3,5-Dihydroxybenzyl alcohol may be employed in the synthesis of dimethylsilyl linked dihydroxybenzyl alcohol based dendrimers, which can exhibit unique properties and find use in specialized applications.
Used in Research and Characterization:
The aggregation behavior of 3,5-dihydroxybenzyl alcohol based dendritic polymers has been investigated using dynamic light scattering and transmission electron microscopy, contributing to the understanding of their properties and potential uses.
Used in the Preparation of Carboxylate-Terminated Dendrimers:
3,5-Dihydroxybenzyl alcohol building block has been described in the preparation of dendritic polyether macromolecules with carboxylate groups as chain-ends, which can be used in various applications, such as catalysis, sensing, and drug delivery.
Check Digit Verification of cas no
The CAS Registry Mumber 29654-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,5 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29654-55:
(7*2)+(6*9)+(5*6)+(4*5)+(3*4)+(2*5)+(1*5)=145
145 % 10 = 5
So 29654-55-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O3/c8-4-5-1-6(9)3-7(10)2-5/h1-3,8-10H,4H2
29654-55-5Relevant articles and documents
Resorcinarenes as templates: A general strategy for the synthesis of large macrocycles
Li, Xuehe,Upton, Thomas G.,Gibb, Corinne L. D.,Gibb, Bruce C.
, p. 650 - 651 (2003)
The concept that resorcinarenes can be used as templates for the synthesis of large macrocycles is introduced. By way of example, previously inaccessible, aromatic crown ethers compounds are synthesized. Copyright
Synthesis of 3, 5 - dihydroxy benzaldehyde method (by machine translation)
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Paragraph 0030-0037, (2019/10/04)
The invention discloses a method for synthesizing 3, 5 - dihydroxy benzaldehyde of the method, the synthetic route is: first 3, 5 - dihydroxy benzoic acid sodium borohydride, dimethyl sulfate, boric acid under the action of the three methyl ester intermediate B obtained, then intermediate B in chromium trioxide and sulfuric acid to obtain compound under the action of the C, i.e. 3, 5 - dihydroxy benzaldehyde; reaction is: The invention of mild synthetic conditions, the reaction yield is high, and the process of the method is simple, the raw material is cheap, simple and convenient operation, is extremely suitable for industrial production, has a very wide range of industrial application and market value. (by machine translation)
Preparation method of 3,5-dihydroxybenzyl alcohol
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Paragraph 0007; 0011; 0013, (2017/05/27)
The invention relates to a preparation method of a medical and chemical intermediate 3,5-dihydroxybenzyl alcohol. The method comprises the following steps of: with commercially available 3,5-dihydroxy-benzoic acid as a raw material, preparing 3,5-diacetoxybenzoic acid through an acetylation reaction; reducing carboxyl into alcohol by a sodium borohydride/iodine borohydride system; and finally, performing acetyl de-protection using a weak base solution to obtain the target product 3,5-dihydroxybenzyl alcohol. The synthesis path has the characteristics of cheap and easily available reagent, mild reaction conditions, easiness in operation, easiness in product separation, relatively high yield and the like.
