61229-07-0

Usage

Uses

Used in Pharmaceutical Industry:
(4E)-6-methylhept-4-enoic acid is used as a building block for the synthesis of various drugs and compounds, contributing to the development of new medications and therapies.
Used in Chemical Industry:
(4E)-6-methylhept-4-enoic acid is used as a precursor for the production of fragrances, flavors, and polymers, enhancing the variety and quality of products in these industries.
Used in Plasticizer Manufacturing:
(4E)-6-methylhept-4-enoic acid is used as a component in the manufacturing of plasticizers, improving the flexibility and durability of plastic materials.
Used in Lubricant Additive Production:
(4E)-6-methylhept-4-enoic acid is used as an additive in the production of lubricants, enhancing their performance and reducing friction in various applications.
Used in Metal Salt Synthesis:
(4E)-6-methylhept-4-enoic acid is used in the synthesis of metal salts, which have various applications in different industries, including as catalysts or in the production of other chemicals.

Upstream product

• 59721-82-3 (E)-1-hydroxy-6-methylhept-4-ene 
• 1115-38-4 rac-4-methylpent-1-en-3-yl acetate 
• 6542-52-5 (2-carboxy-1-isopropyl-cyclopropyl)-acetic acid 
• 17857-14-6 (3-carboxypropyl)(triphenyl)phosphonium bromide 
• 78-84-2 isobutyraldehyde 
• 112375-44-7 (Z)-methyl 6-methylhept-4-enoate 
• 55552-69-7 2-ethylmalonyl dichloride 
• 1826-67-1 vinyl magnesium bromide 
• 101971-24-8 (Z)-1-hydroxy-6-methylhept-4-ene 
• 565-68-4 4-methylpent-1-yn-3-ol 
• 4798-45-2 4-methyl-pent-1-en-3-ol 
• 179617-47-1 trans-6-methyl-hept-4-enoic acid ethyl ester 
• 112375-56-1 (E)-methyl 6-methylhept-4-enoate 

Downstream Products

• 112375-59-4 trans-6-methylhept-4-enoic acid chloride 
• 110-15-6 succinic acid 
• 144-62-7 oxalic acid 
• 656234-70-7 (4R,5S)-4-methyl-3-[(4E)-6-methylhept-4-enyl]-5-phenyl-1,3-oxazolidin-2-one 
• 61229-09-2 (Z)-6-Methyl-hept-4-enoic acid 4-hydroxy-3-methoxy-benzylamide 
• 112375-59-4 (Z)-6-Methyl-hept-4-enoyl chloride 
• 948042-48-6 (4S)-4-benzyl-3-[(4E)-6-methylhept-4-enoyl]oxazolidin-2-one 
• 214286-77-8 (E)-(S)-4-[(2R,5S)-5-Cyclopentylsulfanylcarbonylamino-6-methyl-4-oxo-2-(4-trifluoromethyl-benzyl)-heptanoylamino]-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester 
• 214286-70-1 ethyl-3--L-Phe(4-F)-L-(Tr-Gln)>-E-propenoate 
• 214286-75-6 (E)-(S)-4-[(2R,5S)-5-tert-Butoxycarbonylamino-6-methyl-4-oxo-2-(4-trifluoromethyl-benzyl)-heptanoylamino]-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester 
• 214286-46-1 (E)-(S)-4-((2R,5S)-2-Benzyl-5-cyclopentylsulfanylcarbonylamino-6-methyl-4-oxo-heptanoylamino)-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester 
• 214286-45-0 (E)-(S)-4-((2R,5S)-2-Benzyl-5-benzylsulfanylcarbonylamino-6-methyl-4-oxo-heptanoylamino)-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester 
• 214286-66-5 ethyl-3--L-Phe(4-F)-L-(Tr-Gln)>-E-propenoate 
• 214286-43-8 (E)-(S)-4-((2R,5S)-2-Benzyl-5-tert-butoxycarbonylamino-6-methyl-4-oxo-heptanoylamino)-6-(trityl-carbamoyl)-hex-2-enoic acid ethyl ester 

Relevant academic research and scientific papers

Synthetic method and application of Euproctis pseudoconspersa Strand pheromone

The invention relates to the field of pesticide chemical technology, specifically to a synthetic method of Euproctis pseudoconspersa Strand pheromone. The Euproctis pseudoconspersa Strand pheromone is (R)-10,14-dimethylpentadecaneisobutyrate, which is syn

Enantioselective bromolactonization of cis-1,2-disubstituted olefinic acids using an amino-thiocarbamate catalyst

A facile, highly regio- and enantioselective amino-thiocarbamate-catalyzed bromolactonization of cis-1,2-disubstituted olefinic acids has been developed. The use of the enantio-enriched lactones in the synthesis of chiral synthetic intermediates is also demonstrated. 2012

Antipicornaviral compounds and compositions, their pharmaceutical uses, and materials for their synthesis

Peptido and peptidomimetic compounds of the formula: wherein the formula variables are as defined in the disclosure, advantageously inhibit or block the biological activity of the picornaviral 3C protease. These compounds, as well as pharmaceutical compos

Antipicornaviral compounds compositions containing them and methods for their use

Picornaviral 3C protease inhibitors, obtainable by chemical synthesis, inhibit or block the biological activity of the picornaviral 3C protease. These compounds, as well as pharmaceutical compositions that contain these compounds, are suitable for treatin

Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 3. Structure-activity studies of ketomethylene-containing peptidomimetics

The structure-based design, chemical synthesis, and biological evaluation of various ketomethylene-containing human rhinovirus (HRV) 3C protease (3CP) inhibitors are described. These compounds are comprised of a peptidomimetic binding determinant and an e

A general and stereoselective synthesis of the capsaicinoids via the orthoester Claisen rearrangement

Capsaicin, a main pungent principle of hot pepper, and its 15 analogs have been efficiently synthesized. The key step of this synthetic scheme is the orthoester Claisen rearrangement, which transformed allylic alcohols 2A-C to (E)-alkenoates 3A-C (E/Z > 100) in a highly stereoselective manner. The subsequent carbon chain elongations on 3 based on the cyanation or the malonic acid ester synthesis afforded (E)-alkenoic acids 8, which were converted to the corresponding acid chloride and then coupled with vanillylamine to give capsaicinoids. HPLC and CE (capillary electrophoresis) analyses of these capsaicinoids were also carried out.

Biosynthesis of tetronasin: Part 6. Preparation of structural analogues of the diketide and triketide biosynthetic precursors to tetronasin

The preparation of three analogues of the putative diketide biosynthetic precursor (2) and eight analogues of the putative triketide biosynthetic precursor (3) of the acyl tetronic acid ionophore tetronasin, as N-acetylcysteamine thioesters (4), (5), (6), (12), (13), (14), (15), (22), (23), (24) and (25) is described. Five examples are 19F-labelled; a new, enantiospecific method for the creation of a fluorinated quarternary α-centre is presented.

An Alternate Synthesis of the Capsaicinoids

Five capsaicinoids, the pungent ingredients of hot peppers, have been efficiently synthesized by a method involving the Wittig reaction between isobutyl triphenylphosphorane and the appropriate lactols (3), followed by the nitrous acid-induced isomerization of the resultant (Z)-olefins (4) to (E)-olefins (5).

The Capsaicinoids: Their Separation, Synthesis, and Mutagenicity

Capsaicin (1b), the pungent ingredient in many varietes of Capsicums has recently been implicated as a possible carcinogen.When obtained from natural sources 1b is always accompanied by a number of related homologues.We have isolated seven of these homologues, characterized them, and synthesized them by a general and unique route developed in our laboratories.Also reported are mutagenicity data for 1b and an extract of red pepper as measured by the Ames assay and the V-79 mammalian cell assay.