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2,6-Dipropyl-5-ethyl-1,3-dioxane-4-ol is a chemical compound with the molecular formula C11H22O2. It belongs to the class of compounds known as dioxanes, which are organic compounds containing a 1,3-dioxane moiety, consisting of two oxygen atoms bound to each other at the 1and 3-positions, and a six-member saturated heterocycle. This particular compound is characterized by the presence of two propyl groups and one ethyl group attached to the dioxane ring.

16889-19-3

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16889-19-3 Usage

Uses

Used in Chemical Synthesis:
2,6-Dipropyl-5-ethyl-1,3-dioxane-4-ol is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows it to be a versatile building block for the creation of more complex molecules, making it valuable in the field of organic chemistry.
Used in Research:
2,6-Dipropyl-5-ethyl-1,3-dioxane-4-ol is used as a research compound to study its properties and potential applications. Its presence in the class of dioxanes makes it an interesting subject for investigation, as it may exhibit unique chemical behaviors and interactions with other molecules.
Used in Pharmaceutical Industry:
2,6-Dipropyl-5-ethyl-1,3-dioxane-4-ol is used as a potential candidate for the development of new pharmaceuticals. Its specific properties may offer opportunities for the treatment of various diseases or conditions, and further research is needed to explore its potential in this field.
Used in Material Science:
2,6-Dipropyl-5-ethyl-1,3-dioxane-4-ol is used in the development of new materials with unique properties. Its chemical structure may contribute to the creation of novel materials with applications in various industries, such as electronics, energy storage, or advanced manufacturing.

Check Digit Verification of cas no

The CAS Registry Mumber 16889-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,8 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16889-19:
(7*1)+(6*6)+(5*8)+(4*8)+(3*9)+(2*1)+(1*9)=153
153 % 10 = 3
So 16889-19-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O3/c1-4-7-10-9(6-3)12(13)15-11(14-10)8-5-2/h9-13H,4-8H2,1-3H3

16889-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ethyl-2,6-dipropyl-1,3-dioxan-4-ol

1.2 Other means of identification

Product number -
Other names Cyclohexanol,2,4-dioxa-3,5-dipropyl-6-ethyl

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:16889-19-3 SDS

16889-19-3Upstream product

16889-19-3Relevant academic research and scientific papers

Asymmetric cross- and self-aldol reactions of aldehydes in water with a polystyrene-supported triazolylproline organocatalyst

Llanes, Patricia,Sayalero, Sonia,Rodríguez-Escrich, Carles,Pericàs, Miquel A.

supporting information, p. 3507 - 3512 (2016/07/06)

A polystyrene (PS) immobilized triazolylproline has been prepared by a bottom-up approach involving co-polymerization with full regiocontrol. The resulting PS resin swells in water and has been applied to the enantioselective cross-aldol reaction and to the self-aldol reaction of aldehydes under essentially neat conditions, excellent yields and stereoselectivities being recorded.

COMPOUNDS FOR THE CONTROLLED RELEASE OF ACTIVE ALDEHYDES

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Page/Page column 15-16, (2008/06/13)

The present invention relates to the field of perfumery. More particularly, it concerns an aldoxane derivative of Formula (I) capable of protecting an active aldehyde R1CHO, for example a perfumery or flavor aldehyde, from a chemically aggressive medium into which they have to be added, and then of releasing said active aldehyde at the desired moment. The present invention concerns also the use of said compound in perfumery or in the flavor industry as well as the compositions or articles associated with said aldoxanes.

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