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4461-87-4

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4461-87-4 Usage

Description

1,1-Dimethoxybutane, also known as 1,1-Butylene dimethyl ether, is an organic compound with the chemical formula C6H14O2. It is a colorless liquid with a mild ether-like odor and is commonly used as a solvent and reagent in various chemical processes.

Uses

Used in Chemical Synthesis:
1,1-Dimethoxybutane is used as a solvent and reagent for the preparation of imine type quaternary ammonium salt catalysts. These catalysts are essential in the synthesis of low-viscosity polyisocyanates, which are crucial components in the production of polyurethane materials.
In the Chemical Industry:
1,1-Dimethoxybutane is used as a solvent in the chemical industry for various applications, including the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its ability to dissolve a wide range of substances makes it a versatile and valuable asset in the field.
In the Polymer Industry:
1,1-Dimethoxybutane is used as a component in the production of polyurethane materials, which are widely used in the manufacturing of flexible and rigid foams, adhesives, sealants, coatings, and elastomers. Its role in the synthesis of low-viscosity polyisocyanates contributes to the development of high-quality and versatile polyurethane products.
In the Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 1,1-Dimethoxybutane can also be used in the pharmaceutical industry as a solvent for the synthesis of various drugs and active pharmaceutical ingredients. Its ability to dissolve a wide range of compounds makes it a useful tool in the development and production of medications.

Synthesis Reference(s)

The Journal of Organic Chemistry, 49, p. 2808, 1984 DOI: 10.1021/jo00189a032

Check Digit Verification of cas no

The CAS Registry Mumber 4461-87-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,6 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4461-87:
(6*4)+(5*4)+(4*6)+(3*1)+(2*8)+(1*7)=94
94 % 10 = 4
So 4461-87-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O2/c1-4-5-6(7-2)8-3/h6H,4-5H2,1-3H3

4461-87-4Relevant articles and documents

Kinetische Untersuchungen zur Methanolyse von Acetalen

Claus, P.,Berndt, T.,Scherzer, K.

, p. 1205 - 1216 (2007/10/02)

It has been shown that the acid-catalyzed methanolysis of the diethylacetales RCH(OEt)2 of acetaldehyde (R=CH3), propionaldehyde (R = C2H5), butyraldehyde (R = C3H7) and caprylaldehyde (R = C7H15) at temperatures between 283 and 318 K proceeds as a consecutive reaction involving a reversible second step.The pseudo first order rate constants of the three reaction steps, their activation parameters and equilibrium constants were estimated by measuring the concentration-time-curves of starting product, intermediate and final product and using a large excess of methanol.There is a linear dependence be tween rate constants of methanolysis and concentration of the catalyst.

Ozonolysis of Symmetrically 1,2-Disubstituted Ethylenes in HCl/Methanol Solutions: Acid Catalyzed Reactions of Primary Cleavage Products

Griesbaum, Karl,Neumeister, Joachim

, p. 2697 - 2706 (2007/10/02)

The ozonolysis of olefins in 1 M anhydrous solutions of hydrogen chloride in methanol at /= 0 deg C was investigated.Upon warm-up of the ozonolysis products, the peroxidic primary fragmentation products were converted into non peroxidic end-products by HCl-catalyzed reactions.Cyclopentene (1a) and cyclohexene (1b), e.g., afforded mixtures of the corresponding α,ω-dialdehydebis(dimethyl acetals) (8), dimethyl α,ω-dicarboxylates (9), and methyl ω-aldehyde dimethyl acetal carboxylates (10).Norbornene (1c) gave a mixture of the correspondingly substituted 1,3-cyclopentane compounds (8c - 10c), phenanthrene (22) gave a mixture of methyl 2'-formyl-2-biphenylcarboxylate (24a), 2,2'-biphenyldicarbaldehyde (24b), and dimethyl 2,2'-biphenyldicarboxylate (24c).A reaction scheme was advanced for the rationalization of the types and the distribution of the products.It was partly substantiated by model reactions.

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