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5774-26-5

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5774-26-5 Usage

General Description

1,1-Diethoxyacetone is an organic compound with the chemical formula C7H14O3. It is a colorless liquid that is commonly used in the synthesis of other compounds. It is known for its sweet odor and is highly flammable. 1,1-Diethoxyacetone is commonly used in the production of fragrances, pharmaceuticals, and other industrial chemicals. It is also used as a reagent in organic chemistry reactions, particularly in the formation of carbon-carbon bonds. However, it is important to handle this chemical with caution as it can be hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 5774-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5774-26:
(6*5)+(5*7)+(4*7)+(3*4)+(2*2)+(1*6)=115
115 % 10 = 5
So 5774-26-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O3/c1-4-9-7(6(3)8)10-5-2/h7H,4-5H2,1-3H3

5774-26-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-Diethoxyacetone

1.2 Other means of identification

Product number -
Other names methylglyoxal diethyl acetal

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:5774-26-5 SDS

5774-26-5Relevant articles and documents

The cooperative effect of Lewis and Br?nsted acid sites on Sn-MCM-41 catalysts for the conversion of 1,3-dihydroxyacetone to ethyl lactate

Kim, Kyung Duk,Wang, Zichun,Jiang, Yijiao,Hunger, Michael,Huang, Jun

supporting information, p. 3383 - 3393 (2019/06/24)

Lactic acid and alkyl lactates are widely applied in the production of food, cosmetics, pharmaceuticals, organic synthesis and biodegradable polymers. They can be prepared via one-pot synthesis from renewable trioses, such as dihydroxyacetone (DHA). Br?nsted-Lewis bifunctional solid acids (BAS & LAS) can promote the reaction via a two-step cascade reaction mechanism. BAS catalyses the dehydration of DHA, resulting in the formation of pyruvaldehyde (PA) via the rearrangement of the enol form. Upon alcohol addition, PA can be converted to the desired alkyl lactates at LAS or to pyruvaldehyde hemiacetal (PAHA) at strong BAS. The density and strength control of Br?nsted acid sites (BAS) and Lewis acid sites (LAS) and the optimization of their cooperation are essential for the efficient conversion of trioses to the target products. Here, we prepared a series of Sn-containing mesoporous MCM-41 catalysts with various BAS/LAS ratios by room temperature techniques. Sn-doped [Si]MCM-41 having a lower BAS/LAS ratio in this research shows a high initial selectivity to ethyl lactate (EL) and similar EL yield in 6 hours as the reported best Sn catalyst Sn-grafted [Si]MCM-41/carbon network materials in DHA conversion. A relatively large density of LAS in Sn-doped [Si]MCM-41 causes a fast conversion of PA to EL, while the overall yield has been limited by the BAS density for the DHA conversion. New H-form [Sn]MCM-41, having a suitable density of LAS and weak BAS and an optimized BAS/LAS ratio, provides a 100% yield of ethyl lactate in the catalytic conversion of DHA in ethanol within 30 min, showing a superior performance hitherto.

High-Yield Synthesis of Ethyl Lactate with Mesoporous Tin Silicate Catalysts Prepared by an Aerosol-Assisted Sol–Gel Process

Godard, Nicolas,Vivian, Alvise,Fusaro, Luca,Cannavicci, Lorenzo,Aprile, Carmela,Debecker, Damien P.

, p. 2211 - 2218 (2017/06/27)

An aerosol-assisted sol–gel method is used to prepare mesoporous tin silicate catalysts that exhibit a record activity in the synthesis of ethyl lactate from dihydroxyacetone and ethanol. The method is based on the formation of an aerosol from a solution of precursors and surfactant. During the fast drying of the droplets, the surfactant self-assembles and the Sn-silica matrix is formed by polycondensation reactions. After calcination, the resulting material is composed of a true tin-silicon mixed oxide in the form of spherical microparticles with calibrated mesopores of 5–6 nm. Sn species are incorporated in the silica network, mainly in the form of single sites. This makes these catalysts highly active for the targeted reaction, as shown by record turnover numbers. The catalyst is recyclable and truly heterogeneous as it can be reused for several cycles and it does not leach.

Selective conversion of dihydroxyacetone-ethanol mixture into ethyl lactate over amphoteric ZrO2-TiO2 catalyst

Mylin, Artur M.,Levytska, Svitlana. I.,Sharanda, Mykhailo E.,Brei, Volodymyr V.

, p. 36 - 39 (2014/02/14)

The conversion of dihydroxyacetone in ethanol solution into ethyl lactate over several acidic and amphoteric oxides at 100-160 C was studied. The formation of ethyl lactate with 80-90% selectivity was observed on amphoteric ZrO2-TiO2

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