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7,9-dimethyl-6,10-dioxaspiro[4.5]decane is a cyclic organic compound characterized by a unique spiro structure, which consists of two rings sharing a common atom. In this case, the compound features a spiro[4.5]decane framework with a dioxa bridge, indicating the presence of two oxygen atoms in the ring. The molecule also contains two methyl groups attached to the 7th and 9th carbon atoms, respectively. This specific arrangement of atoms and functional groups endows the compound with distinct chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science.

6413-22-5

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6413-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6413-22-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6413-22:
(6*6)+(5*4)+(4*1)+(3*3)+(2*2)+(1*2)=75
75 % 10 = 5
So 6413-22-5 is a valid CAS Registry Number.

6413-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,9-dimethyl-6,10-dioxaspiro[4.5]decane

1.2 Other means of identification

Product number -
Other names -

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

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More Details:6413-22-5 SDS

6413-22-5Relevant academic research and scientific papers

Stereospecific annulation of hydroxy vinyl ethers. Synthetic application to polyfunctionalized cyclic compounds

Hanaki, Naoyuki,Ishihara, Kazuaki,Kaino, Makoto,Naruse, Yuji,Yamamoto, Hisashi

, p. 7297 - 7320 (1996)

Stereospecific annulation of hydroxy vinyl ethers in the presence of triflic anhydride and tertiary amines and its synthetic application are described. Each 1-hydroxy-2-oxabicyclo(n.4.0)alkane, 2-oxabicyclo(n.4.0)alk-1(6)-ene and 2-oxabicyclo(n.4.0)alk-1(6+n)-ene is stereoselectivity synthesized from the same hydroxy vinyl ether depending on the choice of the reaction conditions (temperature, solvent and tertiary amine). These compounds lead to polyfunctionalized cyclic compounds and some natural product. We propose that this annulation reaction proceeds through a pure S(N)2-like mechanism.

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