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Dibutyl fluoropropanedioate, also known as dibutyl fluoromalonate, is an organic compound with the chemical formula C11H19FO4. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 230.26 g/mol. dibutyl fluoropropanedioate is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is produced through the reaction of dibutyl malonate with fluorine-containing reagents, such as hydrogen fluoride or fluorinating agents. Due to its reactivity and potential applications, dibutyl fluoropropanedioate is an important building block in the chemical industry, enabling the creation of a wide range of products with diverse functionalities.

1598-96-5

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1598-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1598-96-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1598-96:
(6*1)+(5*5)+(4*9)+(3*8)+(2*9)+(1*6)=115
115 % 10 = 5
So 1598-96-5 is a valid CAS Registry Number.

1598-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name dibutyl 2-fluoropropanedioate

1.2 Other means of identification

Product number -
Other names Fluormalonsaeure-dibutylester

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:1598-96-5 SDS

1598-96-5Downstream Products

1598-96-5Relevant academic research and scientific papers

A Convenient Synthesis of 2-Fluoro- and 2-Chloromalonic Esters Mediated by Hypervalent Iodine

Kitamura, Tsugio,Muta, Kensuke,Oyamada, Juzo

, p. 3241 - 3245 (2015/10/19)

Direct fluorination of malonic esters with a reagent system of iodosylbenzene and Et3N·5HF gave the corresponding 2-fluoromalonic esters in good to high yields. Direct chlorination using iodosylbenzene and hydrochloric acid also provided the 2-chloromalonates in high yields.

METHOD OF PRODUCING MONOFLUOROMALONIC ACID DERIVATIVE

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Paragraph 0038-0041, (2017/02/24)

PROBLEM TO BE SOLVED: To provide a method of producing a monofluoromalonic acid ester derivative that has a high yield, facilitates separation of a product, and allows industrial production. SOLUTION: A malonic acid ester derivative (1) is reacted with a hydrogen fluoride source in the presence of an iodosylbenzene derivative or an iodobenzene derivative and an oxidizing agent, to produce a monofluoromalonic acid derivative (4). COPYRIGHT: (C)2015,JPOandINPIT

Efficient synthesis of dissymmetric malonic acid S, O -esters via monoalcoholysis of symmetric dithiomalonates under neutral conditions

Matsuo, Kazumasa,Shindo, Mitsuru

supporting information; experimental part, p. 4406 - 4409 (2011/10/08)

A novel method for the highly selective synthesis of dissymmetric S,O-malonates starting from symmetric diphenyl dithiomalonates under neutral conditions is described. The key step is the thermal formation of an acylketene, the stability of which would co

Preparation des 2-fluoro-3,3-dihalogeno acrylates a partir des alcoxycyclopropanes polyhalogenes

Nguyen, T.,Wakselman, C.

, p. 720 - 725 (2007/10/02)

Route to 2-fluoro-3,3-dihalogenoacrylates via polyhalogenated alkoxycyclopropanes. 3,3-Dichloro- and 3,3-dibromo-2-fluoroacrylates have been prepared from alkoxy-chlorodifluoroethylene via their dihalogenocarbene adducts.The orientation of the cyclopropan

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