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Dihydro-3,3-diethyl-2,5-furandione, also known as 3,3-diethyldihydrofuran-2,5-dione, is an organic compound with the chemical formula C7H12O3. It is a colorless to pale yellow liquid with a molecular weight of 144.17 g/mol. Dihydro-3,3-diethyl-2,5-furandione is characterized by its dihydrofuran structure, which consists of a five-membered ring with two oxygen atoms and three carbon atoms, along with two additional carbon atoms (ethyl groups) attached to the third carbon atom. Dihydro-3,3-diethyl-2,5-furandione is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is typically produced through chemical reactions involving furan derivatives and has applications in the manufacturing of fragrances, flavorings, and other industrial products.

2840-69-9

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2840-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2840-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,4 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2840-69:
(6*2)+(5*8)+(4*4)+(3*0)+(2*6)+(1*9)=89
89 % 10 = 9
So 2840-69-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O3/c1-3-8(4-2)5-6(9)11-7(8)10/h3-5H2,1-2H3

2840-69-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-diethyloxolane-2,5-dione

1.2 Other means of identification

Product number -
Other names 2,2-diethyl-succinic acid anhydride

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:2840-69-9 SDS

2840-69-9Relevant academic research and scientific papers

Synthesis of Cyclic Anhydrides via Ligand-Enabled C–H Carbonylation of Simple Aliphatic Acids

Herron, Alastair N.,Yu, Jin-Quan,Zhuang, Zhe

supporting information, p. 16382 - 16387 (2021/06/23)

The development of C(sp3)–H functionalizations of free carboxylic acids has provided a wide range of versatile C?C and C?Y (Y=heteroatom) bond-forming reactions. Additionally, C–H functionalizations have lent themselves to the one-step preparation of a number of valuable synthetic motifs that are often difficult to prepare through conventional methods. Herein, we report a β- or γ-C(sp3)–H carbonylation of free carboxylic acids using Mo(CO)6 as a convenient solid CO source and enabled by a bidentate ligand, leading to convenient syntheses of cyclic anhydrides. Among these, the succinic anhydride products are versatile stepping stones for the mono-selective introduction of various functional groups at the β position of the parent acids by decarboxylative functionalizations, thus providing a divergent strategy to synthesize a myriad of carboxylic acids inaccessible by previous β-C–H activation reactions. The enantioselective carbonylation of free cyclopropanecarboxylic acids has also been achieved using a chiral bidentate thioether ligand.

Cycloalkylthiazoles

-

, (2008/06/13)

The invention relates to compounds of the formula: STR1 wherein R is hydrogen or lower alkyl, R1, R2, R3 and R4, independently, are hydrogen, lower alkyl, lower alkenyl, cycloalkyl or phenyl unsubstituted or substituted by up to 3 substituents independently selected from lower alkyl, lower alkoxy or halogen, or R1 and R2 taken together with the carbon atom are alkylene of 2 to 5 carbon atoms unsubstituted or substituted by lower alkyl, and n is an integer of from 0 to 3, and, when R1 is different from R2 and/or when R3 is different from R4, enantiomers, diastereomers and racemates thereof and, when R is hydrogen, salts thereof with pharmaceutically acceptable bases. The compounds of formula I and, when R is hydrogen, pharmaceutically exceptable salts thereof are useful as bronchopulmonary agents, for example, in the relief of asthma and allergic reactions.

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