53585-95-8

Basic information

• Product Name: (E)-6-Hydroxy-4-methyl-4-hexenoic acid methyl ester
• Synonyms: (E)-6-Hydroxy-4-methyl-4-hexenoic acid methyl ester
• CAS NO: 53585-95-8
• Molecular Formula: C8H14O3
• Molecular Weight: 158.2
• Mol File: 53585-95-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 212.5±28.0 °C(Predicted)
• Appearance: /
• Density: 1.020±0.06 g/cm3(Predicted)
• PKA: 14.29±0.10(Predicted)
• CAS DataBase Reference: (E)-6-Hydroxy-4-methyl-4-hexenoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-6-Hydroxy-4-methyl-4-hexenoic acid methyl ester(53585-95-8)
• EPA Substance Registry System: (E)-6-Hydroxy-4-methyl-4-hexenoic acid methyl ester(53585-95-8)

Safety Data

• Hazardous Substances Data: 53585-95-8(Hazardous Substances Data)

Usage

General Description

(E)-6-Hydroxy-4-methyl-4-hexenoic acid methyl ester is a chemical compound with the molecular formula C8H14O3. It is a methyl ester of (E)-6-hydroxy-4-methyl-4-hexenoic acid, which is a derivative of butyric acid. (E)-6-Hydroxy-4-methyl-4-hexenoic acid methyl ester is commonly used in the production of flavors and fragrances due to its fruity, pineapple-like aroma. It is also used in the synthesis of pharmaceuticals and other organic compounds. Additionally, (E)-6-Hydroxy-4-methyl-4-hexenoic acid methyl ester may have potential applications in the food industry as a flavoring agent. Overall, this chemical has a variety of industrial and commercial uses due to its desirable aroma and chemical properties.

Upstream product

• 1291070-10-4 methyl (E)-6-((tert-butyldimethylsilyl)oxy)-4-methylhex-4-enoate 
• 960060-33-7 1-(tert-butyldimethylsilyloxy)-3-methylbut-3-en-2-ol 
• 114701-65-4 tert-butyldimethyl((3-methylbut-2-en-1-yl)oxy)silane 
• 556-82-1 3-methyl-2-buten-1-ol 
• 89637-71-8 (E)-3-methyl-6-oxohex-2-en-1-yl benzoate 
• 74-88-4 methyl iodide 
• 27872-60-2 (E)-1-acetoxy-5-carboxy-3-methylpent-2-ene 
• 33431-27-5 6-Trityloxy-4-methylhex-4-ensaeure 
• 37715-33-6 essigsaeure-<(E)-6,7-dihydroxy-3,7-dimethyl-2-octenyl>ester 
• 37715-34-7 1-Trityloxy-6,7-dihydroxy-3,7-dimethyloct-2-en 
• 92464-72-7 (2E)-6,7-epoxy-3,7-dimethyl-1-triphenylmethoxy-2-octene 
• 33431-26-4 6-Trityloxy-4-methylhex-4-enal 
• 35334-60-2 (E)-6-acetoxy-4-methyl-4-hexenal 
• 105-87-3 3,7-dimethyl-2E,6-octadien-1-yl acetate 

Downstream Products

• 34185-71-2 3-(5-carboxy-3-methyl-(2E)-penten-1-yl)-2-methyl-1,4-naphthoquinone 

Relevant articles and documents

ANTICOAGULANT COMPOUNDS AND THEIR USE

According to the invention there is provided a compound of formula (I): wherein R1, R2, R3 and n have meanings given in the description, or a pharmaceutically acceptable solvate, salt or prodrug thereof for use as an anticoagulant.

Chiral Amino Alcohol Accelerated and Stereocontrolled Allylboration of Iminoisatins: Highly Efficient Construction of Adjacent Quaternary Stereogenic Centers

We have developed a highly efficient asymmetric allylboration of ketimines with nonchiral γ,γ-disubstituted allylboronic acids by using a chiral amino alcohol as the directing group, which is otherwise challenging. The amino alcohol not only serves as a cheap source of nitrogen and chirality, but also dramatically enhances the reactivity. The versatility of this method was demonstrated by its ability to access all four stereoisomers with adjacent quaternary carbon centers. A reaction model was proposed to explain the diastereoselectivity and the rate-accelerating effect.

A convergent synthesis of mycophenolic acid

A new method for the synthesis of Mycophenolic acid using a convergent approach has been developed where the key step is a palladium mediated allyl-aryl tin coupling.