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16889-19-3

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16889-19-3 Usage

General Description

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 1- and 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. It is primarily used in research and chemical synthesis, and its specific properties and applications may vary depending on the context and the intended use.

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 articles and documents

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.

Aldol Condensations Promoted by a Tetraalkoxysilane in the Presence of Fluoride Ions

Chuit, C.,Corriu, R. J. P.,Reye, C.

, p. 294 - 297 (2007/10/02)

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