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6-(Prop-2-en-1-yl)-1,4-dioxaspiro[4.5]decane is a complex organic chemical compound with the molecular formula C9H14O2. It is a derivative of 1,4-dioxaspiro[4.5]decane, featuring a prop-2-en-1-yl group attached to the 6th carbon atom. 6-(prop-2-en-1-yl)-1,4-dioxaspiro[4.5]decane is characterized by a spiro structure, which consists of two cyclic structures connected through a common atom. The presence of the 1,4-dioxaspiro[4.5]decane core provides the molecule with unique properties, such as a strained ring system and a high degree of conformational flexibility. The prop-2-en-1-yl group introduces a double bond, which can participate in various chemical reactions, such as addition or polymerization. 6-(prop-2-en-1-yl)-1,4-dioxaspiro[4.5]decane has potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals, as well as in materials science for the development of new polymers and materials with unique properties.

6126-55-2

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6126-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6126-55-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6126-55:
(6*6)+(5*1)+(4*2)+(3*6)+(2*5)+(1*5)=82
82 % 10 = 2
So 6126-55-2 is a valid CAS Registry Number.

6126-55-2SDS

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 6-prop-2-enyl-1,4-dioxaspiro[4.5]decane

1.2 Other means of identification

Product number -
Other names 6-(prop-2-en-1-yl)-1,4-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

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More Details:6126-55-2 SDS

6126-55-2Relevant academic research and scientific papers

Synthesis and conformational analysis of macrocyclic dilactones mimicking the pharmacophore of aplysiatoxin

Knust, Henner,Hoffmann, Reinhard W.

, p. 1871 - 1893 (2007/10/03)

A small number of macrocyclic dilactones of type 3, i.e., 9, 10, 11, and epi-11, comprising a 3,4-dihydroxypentanoic acid unit, the pharmacophore of aplysiatoxin, and a conformationally preorganized ω-hydroxynonanoic acid unit were synthesized. Conformati

Ozonolysis of Enol Ethers. 9. Synthesis and Ozonolysis of 5,6,7,8-Tetrahydrochroman

Schank, Kurt,Beljan, Petra

, p. 558 - 561 (2007/10/03)

The regioselectivity of the transfer of three oxygens of ozone to the olefinic carbons of the rigid substituted enol ether 5,6,7,8-tetrahydrochroman (3) is proved by isolation of ω-caprinolactone 5 instead of an earlier claimed oxacyclodecanone 4.

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