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Dibutyl malonic acid is an organic compound with the chemical formula C10H18O4. It is a diester of malonic acid, where the two hydrogen atoms of malonic acid are replaced by butyl groups. This colorless liquid is soluble in organic solvents and is commonly used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Dibutyl malonic acid is also known for its potential applications in the production of polymers and as a reagent in organic synthesis. Its properties, such as its reactivity and solubility, make it a valuable component in the development of new chemical compounds and materials.

2283-16-1

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2283-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2283-16-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,8 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2283-16:
(6*2)+(5*2)+(4*8)+(3*3)+(2*1)+(1*6)=71
71 % 10 = 1
So 2283-16-1 is a valid CAS Registry Number.

2283-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dibutylpropanedioic acid

1.2 Other means of identification

Product number -
Other names Di-n-butyl-malonsaeure

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:2283-16-1 SDS

2283-16-1Relevant academic research and scientific papers

Improved synthesis and low-temperature performance of a series of saturated α-branched fatty acids

Jiang, Yang,Hu, Wenjing,Xu, Jian,Li, Jiusheng

, p. 2359 - 2363 (2017)

Five saturated α-branched fatty acids, also known as Guerbet acids, including α-propylhexyl acid (G 1 ), α-butylhexyl acid (G 2 ), α-propyloctyl acid (G 3 ), α-butyloctyl acid (G 4 ), and α-hexyloctyl acid (G 5 ), were synthesized in high yields by four-step reaction. Colorless, almost odorless, and oily products were obtained with high purity, whose structures were confirmed by GC, 1H/13C NMR, and ESI-MS characterization. G 1, G 3, and G 4 had pour points lower than -60 °C, while G 2 and G 5 showed higher pour points (-42 °C and 6 °C, respectively) because of their molecular symmetry. Considering the low-temperature properties, G 1, G 3, G 4, and even G 2 held great potential applications in the lubricant and oilfield.

Method for preparing Guerbet acids by taking malonate as raw material

-

Paragraph 0025, (2017/08/29)

The invention discloses a method for preparing Guerbet acids by taking malonate as a raw material. The method comprises the following steps: using the malonate as the raw material, and carrying out alkylation reaction under the action of alkali to obtain dialkyl malonate; sequentially carrying out hydrolysis reaction and decarboxylic reaction on obtained dialkyl malonate to obtain the Guerbet acid, wherein the malonate is dimethyl malonate or diethyl malonate; the alkali of the alkylation reaction is selected from one or more of potassium carbonate, sodium hydroxide, potassium hydroxide, sodium methylate and sodium ethoxide; an alkylating reagent is haloalkane with 2 to 20 carbons. According to the method disclosed by the invention, the Guerbet acids are prepared by taking the malonate as the raw material for the first time; related three reactions are easily operated, high temperature or high pressure is not needed, and high yield is realized; by means of the alkylation reaction disclosed by the invention, a main chain structure and a branched chain structure of the Guerbet acids can be flexibly regulated and controlled, and further the Guerbet acids with different properties are obtained.

Microwave assisted hydrolysis of Meldrum's acid derivatives and decarboxylation of derived malonic acids

Helavi,Solabannavar,Desai,Mane

, p. 174 - 175 (2007/10/03)

Microwave induced hydrolysis of alkyl Medrum's acids and decarboxylation of derived malonic acids using poly-4-vinylpyridine as a catalyst gives high yields of carboxylic acids in a short time.

Role of Substituents in Copper(II) Extraction with N,N'-Bis(8-quinolyl)malonamides

Hirose, Takuji,Hiratani, Kazuhisa,Kasuga, Kazuyuki,Saito, Kiyoshi,Koike, Tohru,et al.

, p. 2679 - 2684 (2007/10/02)

It has been found that substituents on N,N'-bis (8-quinolyl)malonamide play an important role in copper(II) extraction: among the substituents studied, benzyl groups dramatically increased extractability of the malonamide complex.The role of substituents is discussed on the basis of the results of titration and 1H NMR measurements of copper(II) or nickel(II) complexes as well as copper(II)-extraction experiments.Intramolecular interactions between ? electrons of the benzyl group and the metal centre of the complex are proposed to occur.

1,1-Alkanediol dicarboxylate linked antibacterial agents

-

, (2008/06/13)

Useful antibacterial agents in which a penicillin and/or a beta-lactamase inhibitor are linked via 1,1-alkanediol dicarboxylates are of the formula STR1 where A is the residue of certain dicarboxyic acids, R3 is H or (C1 -C3), n is zero or 1 such that when n is zero R is P or B and R1 is the residue of certain esters, H or a salt thereof; and when n is 1, one of R and R1 is P and the other is B, and P is STR2 where R2 is H or certain acyl groups, and B is the residue of a beta-lactamase inhibiting carboxylic acid; a method for their use, pharmaceutical compositions thereof and intermediates useful in their production.

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