3-Oxaspiro[5.5]undecane-2,4-dione


Chemical Name: 3-Oxaspiro[5.5]undecane-2,4-dione
CAS Number: 1010-26-0
Product Number: AG0003GL(AGN-PC-0KK6H2)
Synonyms:
MDL No:
Molecular Formula: C10H14O3
Molecular Weight: 182.2164

Identification/Properties


Properties
MP:
67-70 °C
BP:
336 °C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
182.219g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
182.094g/mol
Monoisotopic Mass:
182.094g/mol
Topological Polar Surface Area:
43.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
221
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


Request for Quotation


Customer Feedback


Chemical Structure



1,1-Cyclohexanediacetic Anhydride, also known as CHDA Anhydride, is a versatile compound widely used in chemical synthesis. Its unique molecular structure makes it a valuable reagent in various reactions, particularly in the field of organic chemistry.When utilized in chemical synthesis, 1,1-Cyclohexanediacetic Anhydride serves as a key building block for the formation of complex organic molecules. Its cyclic anhydride structure allows for controlled and selective reactions, making it an ideal reagent for the modification of functional groups in organic compounds.One of the significant applications of 1,1-Cyclohexanediacetic Anhydride is in the synthesis of pharmaceutical intermediates and fine chemicals. By reacting with a variety of nucleophiles or electrophiles, this compound can lead to the creation of structurally diverse compounds with potential biological activities. Additionally, its use in the preparation of chiral compounds highlights its importance in asymmetric synthesis techniques.Furthermore, the reactivity of 1,1-Cyclohexanediacetic Anhydride enables it to participate in key transformations such as acylation, amidation, and cyclization reactions. This versatility allows chemists to access a wide range of chemical structures, facilitating the development of new materials, drugs, and agrochemicals.In conclusion, the utility of 1,1-Cyclohexanediacetic Anhydride in chemical synthesis lies in its ability to act as a multifunctional reagent for the construction of complex organic molecules with diverse applications across various industries.