4H-Pyran-4,4-dicarboxylic acid, tetrahydro-, dimethyl ester


Chemical Name: 4H-Pyran-4,4-dicarboxylic acid, tetrahydro-, dimethyl ester
CAS Number: 149777-00-4
Product Number: AG001M0B(AGN-PC-0NF9VX)
Synonyms:
MDL No: MFCD02093499
Molecular Formula: C9H14O5
Molecular Weight: 202.2045

Identification/Properties


Properties
BP:
238.2°C at 760 mmHg
Storage:
2-8℃;
Form:
Liquid
Refractive Index:
1.4530 to 1.4560
Computed Properties
Molecular Weight:
202.206g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
202.084g/mol
Monoisotopic Mass:
202.084g/mol
Topological Polar Surface Area:
61.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
211
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


NMR Spectrum


Other Analytical Data


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Chemical Structure



Dimethyl tetrahydropyran-4,4-dicarboxylate, commonly known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it a valuable building block in the creation of various organic molecules.One of the key applications of Dimethyl tetrahydropyran-4,4-dicarboxylate in chemical synthesis is its role as a protective group for alcohols. By selectively blocking the hydroxyl groups in alcohols using $name$, chemists can prevent unwanted reactions from occurring at these sites. This protection allows for the manipulation of other functional groups within a molecule without affecting the alcohol groups, enabling the synthesis of complex organic compounds with precision.Additionally, Dimethyl tetrahydropyran-4,4-dicarboxylate is often utilized as a reagent in the formation of lactones and esters. Its ability to undergo ring-opening reactions makes it a useful tool for introducing cyclic structures into molecules, expanding the synthetic possibilities in organic chemistry. By incorporating $name$ into synthetic routes, chemists can access a diverse array of compounds with tailored properties and functionalities.Overall, Dimethyl tetrahydropyran-4,4-dicarboxylate plays a crucial role in chemical synthesis by serving as a versatile building block, protective group, and reagent. Its applications extend across various disciplines within the field of organic chemistry, making it an indispensable tool for the creation of novel and complex molecules.