36669-06-4 Usage
Description
DiMethyl 2-Hydroxyisophthalate is an organic compound that serves as a key intermediate in the synthesis of various complex molecules and materials. It is characterized by its chemical structure, which includes a central isophthalate core with two methyl groups and a hydroxyl group attached. This unique structure endows it with specific reactivity and properties that make it valuable in the field of organic chemistry and material science.
Uses
Used in Organic Synthesis:
DiMethyl 2-Hydroxyisophthalate is used as a reactant for the synthesis of calix[2]phenol[2]pyrrole 4, a complex organic molecule with potential applications in various fields. Its unique structure allows for the formation of this molecule, which may have properties that are beneficial for specific applications.
Used in Chemical Research:
DiMethyl 2-Hydroxyisophthalate can be utilized in chemical research to explore new reactions and develop novel synthetic pathways. Its reactivity and structural features make it an interesting candidate for studying various chemical transformations and understanding the underlying mechanisms.
Used in Material Science:
In the field of material science, DiMethyl 2-Hydroxyisophthalate may be employed as a building block for the development of new materials with specific properties. Its incorporation into larger structures could lead to materials with enhanced performance characteristics, such as improved stability, reactivity, or selectivity.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, DiMethyl 2-Hydroxyisophthalate could potentially be used in the pharmaceutical industry as a starting material for the synthesis of drug candidates. Its unique structure and reactivity may enable the development of new drugs with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 36669-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,6 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36669-06:
(7*3)+(6*6)+(5*6)+(4*6)+(3*9)+(2*0)+(1*6)=144
144 % 10 = 4
So 36669-06-4 is a valid CAS Registry Number.
36669-06-4Relevant articles and documents
Tetramethyl 3,7-Dihydroxybicyclonona-2,6-diene-2,4,6,8-tetracarboxylate: A Useful Companion to Meerwein's Ester. Topological Analysis of Bicyclononane Synthesis
Bertz, Steven H.
, p. 3585 - 3592 (1985)
The pH dependence of the condensation of dimethyl 3-oxoglutarate and malondialdehyde to produce 2,6-bis(methoxycarbonyl)phenol and tetramethyl 3,7-dihydroxybicyclonona-2,6-diene-2,4,6,8-tetracarboxylate has been studied in detail: the yield of the former is maximal at pH 4,5, the latter at pH 7.5.The hydrolysis-decarboxylation of the latter provides a convenient route to bicyclononane-3,7-dione.The mechanism proposed for this reaction of malonodialdehyde is also relevant to the chemistry of glyoxal and dimethyl 3-oxoglutarate.The retrosynthetic analysis of the bicyclononane skeleton is considered from a topological perspective.
Enhancement of the carbamate activation rate enabled syntheses of tetracyclic benzolactams: 8-oxoberbines and their 5- And 7-membered C-ring homologues
Kurouchi, Hiroaki
supporting information, p. 653 - 658 (2021/02/06)
A route to the direct amidation of aromatic-ring-tetheredN-carbamoyl tetrahydroisoquinoline substrates was developed. This route enabled general access to 8-oxoberberines and their 5- and 7- membered C-ring homologues. It overcomes the undesired tandem side-reactions that result in the destruction of the isoquinoline backbone, which inevitably occurred under our previously reported superacidic carbamate activation method.
Labile linkage for compound delivery to a cell
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Page/Page column 7, (2010/02/11)
Described are ortho carboxy phenol derived acetals and compositions containing ortho carboxy phenol derived acetals which are useful for delivering biologically active compounds to cells. The acetals can be used to reversibly link up to three different mo
