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5413-48-9

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5413-48-9 Usage

General Description

"2,3-dimethyl-1,4-dioxaspiro[4.5]decane" is a chemical compound with the molecular formula C8H14O2 and a spirocyclic structure. It is a colorless liquid that is mainly used as a fragrance ingredient in the production of perfumes, colognes, and other scented products. It has a floral and citrus aroma and is often found in personal care and household products. Additionally, it may also be used as a solvent in certain industrial applications. However, due to its potential for skin and eye irritation, it should be handled with care and proper safety precautions. 2,3-dimethyl-1,4-dioxaspiro[4.5]decane is not known to be harmful to the environment or to have any adverse effects on human health when used in accordance with safety guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 5413-48-9 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 5413-48:
(6*5)+(5*4)+(4*1)+(3*3)+(2*4)+(1*8)=79
79 % 10 = 9
So 5413-48-9 is a valid CAS Registry Number.

5413-48-9SDS

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 2,3-dimethyl-1,4-dioxaspiro[4.5]decane

1.2 Other means of identification

Product number -
Other names 2,3-dimethyl-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

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

More Details:5413-48-9 SDS

5413-48-9Relevant articles and documents

Synthese d'acetals cycliques dans des conditions douces; Applications a l'acetalisation du chloramphenicol

Meslard, J. C.,Subira, F.,Vairon, J. P.,Guy, A.,Garreau, R.

, p. 84 - 89 (2007/10/02)

Acetalization of 1-2 and 1-3 diols, even as sterically crowded as chloramphenicol, by carbonyl derivatives with substituents of various sizes has been performed at room temperature under mild conditions, by using heterogeneous catalysis (sulfonated polystyrene) in the presence of molecular sieves.Several new acetals of chloramphenicol have thus been obtained in good yields, isolated and characterized.

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