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1,3-Dioxane-4,6-dione, 5-(cyclohexylhydroxymethylene)-2,2-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132415-06-6

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132415-06-6 Usage

Structure

Cyclic diester with a dioxane ring and a cyclohexylhydroxymethylene group

Common uses

a. Curing agent in the production of epoxy resins
b. Building block for the synthesis of various organic compounds

Functionality

Ability to crosslink with various molecules

Applications

a. Production of adhesives
b. Coatings
c. Composites

Safety precautions

a. Harmful if ingested or inhaled
b. Can cause skin and eye irritation
c. Handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 132415-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,1 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132415-06:
(8*1)+(7*3)+(6*2)+(5*4)+(4*1)+(3*5)+(2*0)+(1*6)=86
86 % 10 = 6
So 132415-06-6 is a valid CAS Registry Number.

132415-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[cyclohexyl(hydroxy)methylidene]-2,2-dimethyl-1,3-dioxane-4,6-dione

1.2 Other means of identification

Product number -
Other names -

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:132415-06-6 SDS

132415-06-6Relevant academic research and scientific papers

Electrochemical synthesis of versatile ammonium oxides under metal catalyst-, exogenous-oxidant-, and exogenous-electrolyte-free conditions

Yuan, Yong,Li, Liang-Sen,Zhang, Lin,Wang, Feng,Jiang, Lin,Zuo, Lin,Wang, Qi,Hu, Jian-Guo,Lei, Aiwen

supporting information, p. 2768 - 2771 (2021/03/23)

An electrochemical oxidative cross-coupling reaction between 2.5-substituted-pyrazolin-5-ones and ammonium thiocyanate has been developed, which resulted in a series of unprecedented cross-coupling products under metal catalyst-, exogenous-oxidant-, and exogenous-electrolyte-free conditions. It is worth noting that since the resulting cross-coupling products are nearly insoluble in MeCN, the pure product could be afforded without silica gel column purification. In addition, the prepared ammonium oxides are versatile building blocks for synthesizing functionalized pyrazole derivatives.

Creation through immobilization: A new family of high performance heterogeneous bifunctional iminophosphorane (BIMP) superbase organocatalysts

Goldys, Anna M.,Nez, Marta G.,Dixon, Darren J.

supporting information, p. 6294 - 6297 (2015/02/05)

An immobilized chiral bifunctional iminophosphorane superbase organocatalyst has been developed and applied in a range of challenging enantioselective reactions. A unique feature of this novel catalytic system is that the final step creation of the iminophosphorane occurs at the point of immobilization. The utility of the immobilized catalyst system was demonstrated in the nitro-Mannich reaction of ketimines as well as the conjugate addition of high pKa 1,3-dicarbonyl pro-nucleophiles to nitrostyrene. Catalyst recycling was also demonstrated.

Asymmetric total synthesis of the indole alkaloid cyclopiazonic acid and first structure-activity data

Beyer, W.R. Christian,Woithe, Katharina,Lüke, Bettina,Schindler, Michael,Antonicek, Horst,Scherkenbeck, Jürgen

experimental part, p. 3062 - 3070 (2011/05/17)

The indole alkaloid α-cyclopiazonic acid (CPA) is one of the few known inhibitors of sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) besides the terpenoids thapsigargin and artemisinin. We report here the first asymmetric total synthesis of cy

Solid-phase synthesis of substituted pyrazolones from polymer-bound β-keto esters

Tietze, Lutz F.,Evers, Holger,Hippe, Thomas,Steinmetz, Adrian,T?pken, Enno

, p. 1631 - 1634 (2007/10/03)

Polymer-bound acetoacetate 3 was γ-mono- and γ-dialkylated, as well as α-monoalkylated, to give 6, 9, and 13, respectively. Treatment with hydrazine or substituted hydrazines followed by thermal or acidic cyclizing cleavage yielded the pyrazolones 17a-dd in a purity of >90%.

A novel route to 5-substituted 3-isoxazolols. Cyclization of N,O-diBoc β-keto hydroxamic acids synthesized via acyl Meldrum's acids

Sorensen, Ulrik S.,Falch, Erik,Krogsgaard-Larsen, Povl

, p. 1003 - 1007 (2007/10/03)

3-Isoxazolols are most often synthesized from a β-keto ester and hydroxylamine. This cyclization typically gives rise to a major byproduct, the corresponding 5-isoxazolone. We have found that N,O-diBoc-protected β- keto hydroxamic acids can be synthesized and cyclized to 5-substituted 3- isoxazolols without formation of any byproduct. We present a novel and versatile three-step procedure in which carboxylic acid derivatives are converted into acyl Meldrum's acids which, upon aminolysis with N,O-bis(tert- butoxycarbonyl)hydroxylamine, lead to the N,O-diBoc-protected β-keto hydroxamic acids. These hydroxamic acid analogues were then, upon treatment with hydrochloric acid, cyclized to the corresponding 5-substituted 3- isoxazolols.

Decarboxylative elimination of enol triflates as a general synthesis of acetylenes

Fleming, Ian,Ramarao, Chandrashekar

, p. 1113 - 1114 (2007/10/03)

Decarboxylative elimination of a range of enol triflates of β-keto esters gives acetylenes.

Solid-phase synthesis of polymer-bound β-ketoesters and their application in the synthesis of structurally diverse pyrazolones

Tietze, Lutz F.,Steinmetz, Adrian,Balkenhohl, Friedhelm

, p. 1303 - 1306 (2007/10/03)

An efficient solid-phase synthesis of different polymer-bound β-ketoesters 7 is described using readily available acid chlorides 1 and haloalkanes 6 as building blocks. The corresponding pyrazolones 9 and 10 were obtained by mild acid catalyzed reaction with phenylhydrazine or by treatment with hydrazine under cyclisation and cleavage from the resin in high purity and good yield.

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