26825-94-5

Basic information

• Product Name: METHYL 10-BROMODECANOATE
• Synonyms: METHYL 10-BROMODECANOATE, TECH, 90%;10-Bromodecanoic acid methyl ester;Methyl 10-bromodecanoate 90%, technical grade;METHYL 10-BROMODECANOATE
• CAS NO: 26825-94-5
• Molecular Formula: C₁₁H₂₁BrO₂
• Molecular Weight: 265.19
• Product Categories: C10 to C11;Carbonyl Compounds;Esters
• Mol File: 26825-94-5.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 186 °C(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 1.137 g/mL at 25 °C(lit.)
• Refractive Index: n20/D 1.464(lit.)
• CAS DataBase Reference: METHYL 10-BROMODECANOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 10-BROMODECANOATE(26825-94-5)
• EPA Substance Registry System: METHYL 10-BROMODECANOATE(26825-94-5)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 26825-94-5(Hazardous Substances Data)

Usage

General Description

Methyl 10-bromodecanoate is a chemical compound with the molecular formula C11H21BrO2. It is an ester, specifically the methyl ester of 10-bromodecanoic acid. METHYL 10-BROMODECANOATE is used in the synthesis of various organic compounds, and it is also utilized in the production of flavors and fragrances. Methyl 10-bromodecanoate is a colorless to pale yellow liquid with a fruity odor, and it is flammable. It should be handled and stored with proper care and in accordance with standard safety protocols.

Upstream product

• 67-56-1 methanol 
• 50530-12-6 10-bromodecanoic acid 
• 186581-53-3 diazomethane 
• 112-47-0 1,10-Decanediol 
• 7664-93-9 sulfuric acid 
• 51795-88-1 1-bromo-10-(tetrahydropyranyloxy)decane 
• 1679-53-4 10-hydroxydecanoic acid 
• 2640-94-0 methyl 10-hydroxydecanoate 

Downstream Products

• 95259-35-1 10-(2-Nitro-phenylselanyl)-decanoic acid methyl ester 
• 25601-41-6 methyl 9-decenoate 
• 14811-73-5 10-oxo-decanoic acid methyl ester 
• 1642-49-5 dec-9-ynoic acid 
• 65371-24-6 phoracantholide I 
• 14436-32-9 dec-9-enoic acid 
• 1422-27-1 9-hydroxydecanoic acid 
• 134781-57-0 S-Phenyl 9-Hydroxydecanethioate 
• 137743-35-2 10-(3,4-Diphenyl-pyrazol-1-yl)-decanoic acid 
• 137743-37-4 10-(4,5-Diphenyl-pyrazol-1-yl)-decanoic acid 
• 134781-61-6 Pentachlorophenyl 9-Azidodecanoate 
• 134701-90-9 10-(3,4,5-Triphenyl-pyrazol-1-yl)-decanoic acid 
• 1197048-12-6 (S,S)-N-formyl-N-α-methylbenzyl-3-(9'-carbomethoxynonyloxy)amphetamine 
• 50530-12-6 10-bromodecanoic acid 

Relevant articles and documents

Photocatalyic Appel reaction enabled by copper-based complexes in continuous flow

A copper-based photocatalyst, Cu(tmp)(BINAP)BF4, was found to be active in a photoredox Appel-type conversion of alcohols to bromides. The catalyst was identified from a screening of 50 complexes and promoted the transformation of primary and secondary alcohols to their corresponding bromides and carboxylic acids to their anhydrides. The protocol was also amendable and optimized under continuous flow conditions.

INHIBITORS OF BIOFILM FORMATION OF GRAM-POSITIVE AND GRAM-NEGATIVE BACTERIA

The present invention relates to the use of compounds as broad spectrum inhibitors of bacterial biofilm formation. In particular the invention refers to a family of compounds that block the quorum sensing system of Gram-negative and Gram-positive bacteria, a process for their manufacture, pharmaceutical compositions containing them and to their use for the treatment and prevention of bacterial damages and diseases, in particular for diseases where there is an advantage in inhibiting quorum sensing regulated phenotypes of pathogens.

Identification and biosynthesis of (E,E) -10,12-Tetradecadienyl acetate in spodoptera littoralis female sex pheromone gland

A miner component of the sex pheromone gland of the Egyptian cotton leafworm, Spodoptera littoralis, has been identified as (E,E)-10,12-tetradecadienyl acetate. Structural elucidation has been carried out by isobutane-chemical ionization mass spectrometry of the fatty acyl biosynthetic precursor-derived methyl ester. To assign the stereochemistry of the double bonds, the four isomers of both 10,12-tetradecadienyl acetates and methyl 10,12-tetradecadienoates have been synthesized and their gas chromatography retention times and mass spectra have been compared to those of the corresponding natural compounds. Mass-labeling experiments showed that the (E,E)-10,12-tetradecadienoyl moiety is biosynthetically derived from (Z)-11-tetradecenoic acid in the insect pheromone gland.