3,3-dimethyl-1,5-dioxaspiro[5.5]undecane

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3,3-dimethyl-1,5-dioxaspiro[5.5]undecane

  • Name 3,3-dimethyl-1,5-dioxaspiro[5.5]undecane
  • CAS 707-29-9
  • Purity 99%
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What is the 3,3-dimethyl-1,5-dioxaspiro[5.5]undecane ?

3,3-dimethyl-1,5-dioxaspiro[5.5]undecane is , while it's Molecular Formula is C11H20 O2.

What is the CAS number for 3,3-dimethyl-1,5-dioxaspiro[5.5]undecane ?

The CAS number of 3,3-dimethyl-1,5-dioxaspiro[5.5]undecane is 707-29-9.

More information of 3,3-dimethyl-1,5-dioxaspiro[5.5]undecane 707-29-9 are:

Synonyms

2,2-Pentamethylene-5,5-dimethyl-m-dioxane;3,3-Dimethyl-1,5-dioxaspiro[5.5]undecane; 5,5-Dimethyl-1,3-dioxane-2-spirocyclohexane;NSC 7021

CAS?Number

707-29-9

Molecular Formula

C11H20 O2

Molecular Weight

184.279

Density

0.98g/cm3

Boiling Point

214.4°C at 760 mmHg

Flash Point

78.8°C

PSA

18.46000

LogP

2.71980

What is 3,3-dimethyl-1,5-dioxaspiro[5.5]undecane (707-29-9) used for?

3,3-dimethyl-1,5-dioxaspiro[5.5]undecane is a synthetic organic compound characterized by its unique spirocyclic structure. It belongs to the spiroketal class, which is known for their unusual ring structures and a wide range of applications in organic synthesis. 3,3-dimethyl-1,5-dioxaspiro[5.5]undecane features two methyl groups attached to the spirocyclic ring, providing it with a high degree of steric hindrance. Its distinctive structural features make it an interesting target for the development of new reaction methodologies and a potential pharmaceutical lead compound.
Used in Chemical Research:
3,3-dimethyl-1,5-dioxaspiro[5.5]undecane is used as a building block for the synthesis of more complex molecules, contributing to the advancement of organic chemistry.
Used in Coordination Chemistry:
3,3-dimethyl-1,5-dioxaspiro[5.5]undecane is used as a ligand, playing a crucial role in the formation and stabilization of metal complexes.
Used in Pharmaceutical Development:
3,3-dimethyl-1,5-dioxaspiro[5.5]undecane is used as a potential lead compound for the development of new pharmaceuticals, due to its unique spirocyclic structure and high steric hindrance.

InChI:InChI=1/C11H20O2/c1-10(2)8-12-11(13-9-10)6-4-3-5-7-11/h3-9H2,1-2H3

Articles related to 3,3-dimethyl-1,5-dioxaspiro[5.5]undecane:

Article

Source

Ketalization of ketones to 1,3-dioxolanes and concurring self-aldolization catalyzed by an amorphous, hydrophilic SiO2-SO3H catalyst under microwave irradiation

Barbosa, Sandro L.,Ottone, Myrlene,De Almeida, Mainara T.,Lage, Guilherme L.C.,Almeida, Melina A.R.,Nelson, David Lee,Dos Santos, Wallans T.P.,Clososki, Giuliano C.,Lopes, Norberto P.,Klein, Stanlei I.,Zanatta, Lucas D.

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Graphene-catalyzed transacetalization under acid-free conditions

Nongbe, Medy C.,Oger, Nicolas,Ekou, Tchirioua,Ekou, Lynda,Yao, Benjamin K.,Le Grognec, Erwan,Felpin, Fran?ois-Xavier

, p. 4637 - 4639 (2016/09/23)

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