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106017-77-0

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106017-77-0 Usage

General Description

2,2-Dimethyl-1,3-dioxan-4-one, also known as 4-Oxanone, is a chemical compound with the molecular formula C6H10O2. It is a cyclic ester, often used as a solvent in organic synthesis. It is a colorless and flammable liquid with a fruity, sweet odor. This chemical is commonly used in the production of coatings, adhesives, and pharmaceuticals. It can also be used as a solvent for cellulose derivatives, epoxy resins, and various polymers. Additionally, it can be used as a plasticizer and a crosslinking agent for polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 106017-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,1 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106017-77:
(8*1)+(7*0)+(6*6)+(5*0)+(4*1)+(3*7)+(2*7)+(1*7)=90
90 % 10 = 0
So 106017-77-0 is a valid CAS Registry Number.

106017-77-0SDS

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 2,2-dimethyl-1,3-dioxan-4-one

1.2 Other means of identification

Product number -
Other names 1,3-Dioxan-4-one,2,2-dimethyl

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:106017-77-0 SDS

106017-77-0Downstream Products

106017-77-0Relevant articles and documents

A Spectacular Example of the Importance of Rotational Barriers: The Ionization of Meldrum's Acid

Arnett, Edward M.,Harrelson, John A.

, p. 809 - 812 (2007/10/02)

The free energy of ionization of Meldrum's acid (I) is 11.68 kcal/mol more spontaneous than that of its acyclic analogue, dimethyl malonate.This energy difference must represent one of the largest stereoelectronic effects in the literature of organic chemistry and demands careful elucidation.This paper probes the problem by comparing the effects of various structural contributions to the carbon acidity of Meldrum's acid.The most dramatic effect results from increasing the size of the bislactone ring system.There is a rapid decrease in acidity between the 6-membered and 10-membered ring until the 13-membered ring has the same pKa as dimethyl malonate.The obvious conclusion from the assembled results is that the difference between the acidities Meldrum's acid and the larger ring bislactones or diesters lies in the barrier to rotation around the ester bonds.Over half of the 11.68-kcal/mol effect may be explained empirically through the 3-4-kcal/mol stabilization of the Z conformation of esters relative to the E conformation.Another 3 kcal/mol may be assigned to the cyclization effect seen also in the β-diketone series.

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