4454-18-6

Usage

Uses

Used in Plastics Industry:
2,5-DIMETHYLHEXANEDIOIC ACID is used as a plasticizer for [enhancing the flexibility and workability of plastics] due to its chemical characteristics.
Used in Coatings Industry:
2,5-DIMETHYLHEXANEDIOIC ACID is used as a component in the formulation of coatings for [providing desired properties such as durability and resistance to environmental factors] because of its strong acidity and solubility in water.
Used in Synthetic Lubricants Industry:
2,5-DIMETHYLHEXANEDIOIC ACID is used as a base material in the production of synthetic lubricants for [improving their performance and reducing wear and tear in mechanical applications] due to its stability and solubility properties.

InChI:InChI=1/C8H14O4/c1-5(7(9)10)3-4-6(2)8(11)12/h5-6H,3-4H2,1-2H3,(H,9,10)(H,11,12)

Upstream product

• 1003-38-9 2,5-dimethyltetrahydrofuran 
• 144446-84-4 2,5-dimethyl-adipic acid diethyl ester 
• 5363-70-2 hex-1-ene-2,5-dicarboxylic acid 
• 67101-64-8 2,5-dimethyl-1,6-hexanedial 
• 90003-66-0 α,α'-Dimethyl-β,β'-dichlor-muconsaeure 
• 5453-88-3 ethyl 1-methyl-2-oxocyclopentane-1-carboxylate 
• 79-31-2 isobutyric Acid 
• 7664-93-9 sulfuric acid 
• 7722-84-1 dihydrogen peroxide 
• 848761-77-3 3-cyano-1,3-dimethyl-2-oxo-cyclopentanecarboxylic acid ethyl ester 
• 24774-58-1 2,5-dibromohexane 
• 151-50-8 potassium cyanide 
• 500696-52-6 hexane-2,2,5,5-tetracarboxylic acid tetraethyl ester 
• 51522-93-1 2,5-Dimethyl-hexanedioic acid dibutyl ester 

Downstream Products

• 4041-09-2 2,5-dimethylcyclopentanone 
• 23119-30-4 (E),(E)-2,5-Di(methoxycarbonyl)-hexa-2,4-dien 
• 19550-58-4 (R,R)-2,5-dimethyl-adipic acid dimethyl ester 
• 19550-58-4 (S,S)-2,5-dimethyl-adipic acid dimethyl ester 
• 19550-58-4 dimethyl 2,5-dimethylhexanedioate 
• 63802-30-2 2,5-Dimethyl-hexane-bis-thioic acid di-S-p-tolyl ester 

Relevant academic research and scientific papers

CONJUGATES OF CARTILAGE-HOMING PEPTIDES

Compositions such as pharmaceutical compositions and uses for peptide-drug conjugates are disclosed. Such compositions can deliver a drug, a peptide, or a conjugate thereof to a target region, tissue, structure or cell in cartilage.

Preparation of N-thienyl-chloroacetamides and tetrahydro-thien-3-ylidenimines

The invention provides compounds of formula I STR1 wherein R is C1-4 alkoxy-C2-4 alkyl of which the C1-4 alkoxy group is separated by at least 2 C-atoms from the N-atom to which R is bound, each of R2 and R4 independently is CH3 or C2 H5 and R5 is H or CH3, the preparation of such compounds and the use of such compounds for the preparation of N-(thien-3-yl)-chloroacetamides.

Process for the preparation of N-thienyl-chloroacetamides

The invention provides compounds of formula I wherein R is C1-4alkoxy-C2-4alkyl of which the C1-4alkoxy group is separated by at least 2 C-atoms from the N-atom to which R is bound,each of R2 and R4 independently is CH3 or C2H5, and R5 is H or CH3,the preparation of such compounds and the use of such compounds for the preparation of N-(thien-3-yl)-chloroacetamides.

REACTION BEHAVIOR OF CARBON-CARBON AND CARBON-HYDROGEN BONDS IN SUPER ACIDS. CARBOXYLATION OF ALKYL METHYL KETONES WITH CARBON MONOXIDE AND WATER

In a HF-SbF5 solution at -20 -ca.30 deg C under atmospheric pressure, ketones having alkyl groups with five or more carbon atoms underwent the reaction to give corresponding oxo carboxylic acids without any β-scission processes which occur readily in alkyl cations derived by protolysis of alkalnes with seven or more carbon atoms.Tertiary C-H bond located at δ or further away from the oxo group in the substrates could react exclusively to give (ω-1)-oxo-2,2-dimethyl carboxylic acids at -20 deg C.