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126-84-1

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  • 2,2-Diethoxypropane;2,2-diethoxy-propan;Acetone diethyl ketal;acetonediethylketal; CAS NO.126-84-1

    Cas No: 126-84-1

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126-84-1 Usage

Preparation

To a flask equipped as in Preparation 2-11 and containing 1725 gm (37.5 moles) of ethanol, 18.4 gm (0.058 mole) of mercuric acetate, and 28 ml of 26% boron fluoride etherate (26%) at 30°C is added dropwise over a 15 min period at 45-50°C, 1250 gm (12.5 moles) of isopropenyl acetate. After the reaction 2200 gm of 25% sodium hydroxide is added, the organic layer separated, washed first with 400 ml of 0.01 Ν sodium hydroxide, dried, and distilled to afford 1140 gm (69%), b.p. 110-113 C (760 mm Hg).

Safety Profile

Poison by intraperitoneal route.When heated to decomposition it emits acrid smoke.

Check Digit Verification of cas no

The CAS Registry Mumber 126-84-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 126-84:
(5*1)+(4*2)+(3*6)+(2*8)+(1*4)=51
51 % 10 = 1
So 126-84-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O2/c1-5-8-7(3,4)9-6-2/h5-6H2,1-4H3

126-84-1 Well-known Company Product Price

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  • Aldrich

  • (519618)  2,2-Diethoxypropane  97%

  • 126-84-1

  • 519618-25G

  • 1,356.03CNY

  • Detail

126-84-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Diethoxypropane

1.2 Other means of identification

Product number -
Other names 2,2-diethoxy-propane

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:126-84-1 SDS

126-84-1Relevant articles and documents

Solvent-free synthesis of unsaturated ketones by the Saucy-Marbet reaction using simple ammonium ionic liquid as a catalyst

Wang, Congmin,Zhao, Wenjia,Li, Haoran,Guo, Liping

, p. 843 - 847 (2009)

Simple ammonium ionic liquids are efficient catalysts in promoting Saucy-Marbet reactions of unsaturated alcohols with unsaturated ethers to afford the corresponding unsaturated ketones, eliminating the need for volatile organic solvents. The effect of th

Influence of Solvent and Counterion in the Reactions of Alkoxide Ions with the 2-Nitropropan-2-yl Radical

Russel, Glen A.,Baik, Woonphil

, p. 196 - 198 (1988)

Photostimulated free radical chain reactions between alkoxide ions derived from primary alcohols and XCMe2NO2 (X= Cl, Br, NO2, PhSO2, N3, or p-ClC6H4S) occur to produce Me2C(OR)2 by reaction involving the trapping of Me2C(NO2). by RO-, the decomposition of ROCMe2NO2.- to ROCMe2., and the oxidation of ROCMe2. to Me2C=OR+ by XCMe2NO2.

Synthesis of biodiesel without formation of free glycerol

Vol'eva,Belostotskaya,Komissarova,Koverzanova,Kurkovskaya,Usmanov,Gumerov

, p. 915 - 917 (2015/08/25)

A new approach to the synthesis of biodiesel has been developed on the basis of alcoholysis of a triglyceride in combination with acetalization of glycerol with lower carbonyl compounds or acetals derived therefrom. A model synthesis of biodiesel not involving free glycerol has been accomplished using rapeseed oil and acid catalysts, as well as without a catalyst under generation of ethanol supercritical fluid; in the latter case, monoalkyl glycerol ethers are formed in addition to the expected cyclic ketals.

Cationic gold(I) complexes: Highly efficient catalysts for the addition of alcohols to alkynes

Teles, J. Henrique,Brode, Stefan,Chabanas, Mathieu

, p. 1415 - 1418 (2007/10/03)

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