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DI-N-PROPYL OXALATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

615-98-5

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615-98-5 Usage

Synthesis Reference(s)

Canadian Journal of Chemistry, 53, p. 2530, 1975 DOI: 10.1139/v75-360

Check Digit Verification of cas no

The CAS Registry Mumber 615-98-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 615-98:
(5*6)+(4*1)+(3*5)+(2*9)+(1*8)=75
75 % 10 = 5
So 615-98-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O4/c1-3-5-11-7(9)8(10)12-6-4-2/h3-6H2,1-2H3

615-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dipropyl oxalate

1.2 Other means of identification

Product number -
Other names di-n-Propyl oxalate

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:615-98-5 SDS

615-98-5Relevant academic research and scientific papers

Method for synthesizing symmetric oxalate by using dimethyl oxalate and alcohols in one step

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Paragraph 0039; 0040, (2019/01/06)

The invention relates to a method for synthesizing symmetric oxalate, in particular to a method for synthesizing the symmetric oxalate by using dimethyl oxalate and alcohols in one step. The symmetricoxalate is synthesized by using the dimethyl oxalate and the high carbon alcohols such as ethanol, propanol, butanol and pentanol as reaction raw materials and by adopting a one-step synthesis method. A catalyst used in the method is a mesoporous-microporous composite multifunctional basic catalyst, and has the advantages that mesopores significantly improve the mass transfer efficiency, while micropores significantly enlarge the specific surface area of a carrier and improve the dispersion of an active center. 10% MgO-5% Al2O3-8% Fe2O3/Na-meso-Y is used as the catalyst, the raw material ethanol and the dimethyl oxalate are enabled to be subjected to reaction under the atmospheric pressure at the temperature of 100 DEG C under the condition that the space velocity is 2 h-1, wherein the molar ratio of the raw material ethanol to the dimethyl oxalate is equal to 20 to 1; the selectivity of the product diethyl oxalate is stabilized to be about 82%, and the steady state operation is performed for 1000h; the catalytic activity and the product selectivity are basically unchanged. The whole reaction path has the characteristics of being short in synthetic route, simple in process flow and high in raw material conversion rate and product selectivity, and enabling the catalyst to be stable and non-deactivated.

By using low-temperature co- melt solvent a method of catalytic ester (by machine translation)

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Paragraph 0048; 0049, (2017/01/17)

The invention discloses a method of utilizing low-temperature co- melt solvent catalytic ester method, will be 0.05-0.5 mole of sharemelt solvent of low-temperature co-preprocessing, 1-5 mole of share alcohol and 1-10 mole of share of acid in the reaction vessel, stirring and heating, 25-200 ° C reaction under 2-96h, then the reaction fluid settlement , liquid, organic is accepted after passing an examination the level , get the esterification reaction products of the; reaction after the treatment and recovery of low-temperature co- melt solvent the preprocessing, can be reused. This invention utilizes the easy preparation of low-temperature co- melt solvent the preprocessing of catalytic esterification reaction, the reaction front is homogeneous, can be formed after the reaction of the two-phase reaction in the process of direct dehydration, without adding other dehydrating agent, has the advantages of simple operation, the reaction efficiency is high, corrosion of small equipment, less side reactions, the product quality is good, no pollution to the environment, and the like, it has broad application prospects. (by machine translation)

A kind of preparation method of succinic acid diester

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Paragraph 0069-0071, (2017/01/09)

Disclosed is a method for preparing succinic acid diester, in which levulinic acid or levulinate esters are used as raw materials, molecular oxygen is used as oxygen source, and succinic acid diester is produced by catalytic selective oxidation and esterification reaction. The levulinic acid or levulinate esters used as raw materials in the method can be obtained from biomass such as cellulose, starch, agricultural and forestry residues or the like. The method is a new route for preparing succinic acid diester that does not rely on fossil resourse. As the reaction condition in the process is moderate and has a high succinic acid diester selectivity, it has important application prospect.

Vapor pressures and enthalpies of vaporization of a series of the symmetric linear n -alkyl esters of dicarboxylic acids

Lipp, Svetlana V.,Krasnykh, Eugenii L.,Verevkin, Sergey P.

body text, p. 800 - 810 (2011/11/05)

Vapor pressures and the molar enthalpies of vaporization of the linear aliphatic alkyl esters of dicarboxylic acids R-CO2-(CH 2)n-CO2-R with n = (0 to 4) with R = C 2H5, n-C3H7, and n-C 4H9 have been determined using the transpiration method. A linear correlation of enthalpies of vaporization (at T = 298.15 K) of the esters with the number n and with Kovat's indices has been found, proving the internal consistency of measured data.

A FACILE METHOD OF TRANSESTERIFICATION USING PHOSPHORUS YLID

Hashimoto, Shizunobu,Furukawa, Isao,Kuroda, Tomoyuki

, p. 2857 - 2860 (2007/10/02)

The transesterification of carboxylic esters catalysed with phosphorus ylid under neutral and mild conditions has been investigated.The reactions of esters having an electron withdrawing group with methanol proceeded rapidly and with high yield, whereas the reverse reactions proceeded slowly or not at all.

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