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7-methyl-6,10-dioxaspiro[4.5]decane is a cyclic organic compound characterized by a unique spiro structure, which consists of a central carbon atom connected to two different ring systems. This molecule features a seven-membered ring with two oxygen atoms and a methyl group attached to the seventh carbon. The presence of the oxygen atoms in the ring structure imparts dioxa characteristics, which can influence the compound's reactivity and stability. The 7-methyl-6,10-dioxaspiro[4.5]decane is synthesized through various chemical reactions and is utilized in the pharmaceutical and chemical industries for its potential applications in drug development and as a building block for more complex molecules. Its specific properties, such as solubility and reactivity, make it a valuable compound for further research and development in the field of organic chemistry.

5413-44-5

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5413-44-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5413-44-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5413-44:
(6*5)+(5*4)+(4*1)+(3*3)+(2*4)+(1*4)=75
75 % 10 = 5
So 5413-44-5 is a valid CAS Registry Number.

5413-44-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-methyl-6,10-dioxaspiro[4.5]decane

1.2 Other means of identification

Product number -
Other names 7-methyl-6,10-dioxaspiro[4.5]decane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5413-44-5 SDS

5413-44-5Downstream Products

5413-44-5Relevant academic research and scientific papers

MOR zeolite supported Bronsted acidic ionic liquid: An efficient and recyclable heterogeneous catalyst for ketalization

Li, Zhang-Min,Zhou, Yan,Tao, Duan-Jian,Huang, Wei,Chen, Xiang-Shu,Yang, Zhen

, p. 12160 - 12167 (2014/03/21)

In order to widen the application of ionic liquids as efficient and renewable heterogeneous catalysts, supported ionic liquids (SILs) have received considerable attention. A novel heterogeneous catalyst MOR zeolite supported Bronsted acidic ionic liquid (BAIL@MOR) was therefore prepared, characterized and applied in the ketalization reaction. The influences of reaction temperature, time, and catalyst loading have also been investigated in detail. Combined characterization results of XRD, FT-IR, SEM, TG-DTG and N 2 adsorption-desorption suggested that the BAIL [CPES-BSIM][HSO 4] was successfully immobilized on the surface of MOR zeolite by covalent bonds. Moreover, the catalytic performance tests demonstrated that the catalyst BAIL@MOR exhibited excellent catalytic activities in the ketalization of cyclohexanone with glycol, 1,2-propylene glycol and 1,3-butylene glycol under mild reaction conditions, as comparable with the homogeneous catalysis of the precursors [BSmim][HSO4] and H2SO4. In addition, the catalyst BAIL@MOR was also found to be reusable five times without a significant loss of its catalytic activity. Thus, the heterogeneous catalyst BAIL@MOR can act as a promising candidate for the ketalization reaction.

ANALYTICAL ENANTIOMER SEPARATION OF ALIPHATIC DIOLS AS BORONATES AND ACETALS BY COMPLEXATION GAS CHROMATOGRAPHY

Schurig, V.,Wistuba, D.

, p. 5633 - 5636 (2007/10/02)

Cyclic boronates and acetals of mono- and dialkylsubstituted 1,2-, 2,3- 1,3-and 1,4-diols have been quantitatively separated into enantiomers by complexation gas chromatography utilizing optically active metal chelates.An efficient, precise and sensitive method for determining enantiomeric purities for volatile glycols is thus available.

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