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24332-20-5

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24332-20-5 Usage

Chemical Properties

Colorless transparent liquid

Check Digit Verification of cas no

The CAS Registry Mumber 24332-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,3 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24332-20:
(7*2)+(6*4)+(5*3)+(4*3)+(3*2)+(2*2)+(1*0)=75
75 % 10 = 5
So 24332-20-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H12O3/c1-6-4-5(7-2)8-3/h5H,4H2,1-3H3

24332-20-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2-Trimethoxyethane

1.2 Other means of identification

Product number -
Other names Methoxyacetaldehyde Dimethyl 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:24332-20-5 SDS

24332-20-5Relevant articles and documents

Catalysis and Stability Effect of Solvent Alcohol on the C6 Aldose Conversion toward Tetrose

Hou, Wenrong,Yan, Yueer,Li, Gang,Zhan, Yulu,Feng, Lei,Zhang, Ruohong,Hua Li, Zhen,Zhang, Yahong,Tang, Yi

, p. 4182 - 4188 (2019/09/12)

Conversions of biomass feedstock into various valuable chemicals are of great significance. As a typical route, retro-aldol condensation of monosaccharide greatly expands the variety of biomass-derived platform chemicals via a selective C?C splitting. Herein, we describe a solvent-catalysed strategy to high-selectively accumulate tetrose (four-carbon platform chemical) from C6 aldoses via the retro-aldol/aldol process. We find that alcohol solvents with Lewis acidity facilitate the C?C splitting process of hexose under the catalyst-free condition. The conversion is the fastest in methanol while it is the slowest in isopropanol. The product distribution is greatly influenced by the alcohols through shifting the equilibrium between tetrose and glycolaldehyde (GA). The addition of catalyst only accelerates the reaction rate, and does not change the product distribution. On the one hand, the acetalization of GA with methanol or ethanol shifts the equilibrium from tetrose toward GA, which results in a low yield of tetrose in methanol or ethanol solvent. On the other hand, tetrose can be well accumulated in isopropanol or n-butanol, and the yield of tetrose in isopropanol is higher than in n-butanol because tetrose can be well solvated and stabilized in it. This solvent-dependent reaction strategy provides a new possibility which contributes to the conversion of biomass feedback into valuable platform chemicals and accumulation of target products by utilizing the solvation effect.

Production of methyl levulinate from cellulose: Selectivity and mechanism study

Ding, Daqian,Xi, Jinxu,Wang, Jianjian,Liu, Xiaohui,Lu, Guanzhong,Wang, Yanqin

, p. 4037 - 4044 (2015/07/15)

The alcoholysis of cellulose into methyl levulinate (ML) in methanol media was investigated in the presence of several kinds of acid catalyst. One of the synthesized solid niobium-based phosphate catalysts was found to be highly efficient for the generation of ML, reaching an ML yield as high as 56%, higher than the LA yield (52%) in aqueous solution with the same reaction conditions as those used in our previous study (Green Chem., 2014, 16, 3846-3853). More interestingly, in water, very strong Lewis acid promoted the formation of LA; but in methanol, Br?nsted acid enhanced the formation of ML. In-depth investigation showed that the mechanism and type of intermediates of cellulose alcoholysis in methanol were different from those in water and a high Br?nsted/Lewis acid ratio (known as B/L acid ratio) of solid catalysts is needed to prevent the generation of by-products, namely, methyl lactate and 1,1,2-trimethoxyethane. This new-proposed reaction mechanism affected by the B/L acid ratio was very helpful for the design of efficient catalysts.

Interrupted oligomerization revisited: Simple and efficient one-pot multicomponent approach to versatile synthetic intermediates

Valiulin, Roman A.,Halliburton, Logan M.,Kutateladze, Andrei G.

, p. 4061 - 4063 (2008/02/11)

A novel multicomponent reaction allowing for a one-pot formation of three carbon-carbon bonds has been developed. It is based on in situ generation and anionic dimerization of methylenedithiane and produces a versatile synthetic equivalent of 4-hydroxy-1,3-alkanediones which, among other things, offers expeditious one-pot access to 3(2H)-furanones.

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