14952-06-8

Basic information

• Product Name: (2E)-2-Nonenoic acid methyl ester
• Synonyms: (2E)-2-Nonenoic acid methyl ester;(E)-2-Nonenoic acid methyl ester;ZWNPUELCBZVMDA-CMDGGOBGSA-N
• CAS NO: 14952-06-8
• Molecular Formula: C₁₀H₁₈O₂
• Molecular Weight: 170.25
• Mol File: 14952-06-8.mol
• Article Data: 30

Chemical Properties

• Boiling Point: 67-68 °C(Press: 3 Torr)
• Appearance: /
• Density: 0.8998 g/cm3
• Vapor Pressure: 13.7-19Pa at 20-25℃
• CAS DataBase Reference: (2E)-2-Nonenoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-2-Nonenoic acid methyl ester(14952-06-8)
• EPA Substance Registry System: (2E)-2-Nonenoic acid methyl ester(14952-06-8)

Safety Data

• Hazardous Substances Data: 14952-06-8(Hazardous Substances Data)

Usage

Description

(2E)-2-Nonenoic acid methyl ester, also known as Methyl trans-2-nonenoate, is a volatile compound that has been identified in mango wine. It is an organic ester derived from the carboxylic acid (2E)-2-nonenoic acid and methanol. (2E)-2-Nonenoic acid methyl ester is known for its distinctive aroma and is often associated with fruity and floral scents.

Uses

Used in Flavor and Fragrance Industry:
(2E)-2-Nonenoic acid methyl ester is used as a flavoring agent for its fruity and floral aroma, enhancing the taste and smell of various food and beverage products. Its natural occurrence in mango wine makes it a desirable component in the creation of tropical and fruity flavor profiles.
Used in Cosmetics and Perfumery:
In the cosmetics and perfumery industry, (2E)-2-Nonenoic acid methyl ester is used as a fragrance ingredient to add a pleasant and distinctive scent to personal care products, such as perfumes, lotions, and shampoos. Its fruity and floral notes contribute to the overall sensory experience of these products.
Used in the Wine Industry:
(2E)-2-Nonenoic acid methyl ester is used in the wine industry to enhance the aroma and flavor of mango wine and other fruit-based wines. Its presence in these beverages can contribute to a more complex and enjoyable taste experience for consumers.

Upstream product

• 67-56-1 methanol 
• 629-05-0 n-octyne 
• 201230-82-2 carbon monoxide 
• 111-71-7 heptanal 
• 68872-87-7 Methylselanyl-acetic acid methyl ester 
• 111-66-0 oct-1-ene 
• 85909-00-8 (E)-6,6-Dimethyl-hept-2-enoic acid butylamide 
• 85909-03-1 Butyl-((E)-6,6-dimethyl-hept-2-enoyl)-carbamic acid tert-butyl ester 
• 1067-74-9 Methyl diethylphosphonoacetate 
• 4282-40-0 1-Iodoheptane 
• 172159-96-5 methyl (RS)-2-acetylnonanoate 
• 5927-18-4 trimethyl phosphonoacetate 
• 21204-67-1 methyl (triphenylphosphoranylidene)acetate 
• 42599-17-7 (E)-1-iodo-1-octene 

Downstream Products

• 129042-83-7 rac-methyl 3-(benzylamino)nonanoate 
• 31502-14-4 2-nonenyl alcohol 
• 75899-68-2 (E)-4-Hydroxy-2-nonenal 
• 1402134-65-9 (1E,2E)-1-{2-[3-(trifluoromethyl)phenyl]hydrazono}non-2-en-4-ol 
• 1402134-64-8 (1E,2E)-1-{2-[2-(trifluoromethyl)phenyl]hydrazono}non-2-en-4-ol 
• 1402134-72-8 1-[3,5-bis(trifluoromethyl)phenyl]-6-pentyl-1,6-dihydropyridazine 
• 1402134-71-7 6-pentyl-1-[4-(trifluoromethyl)phenyl]-1,6-dihydropyridazine 
• 1402134-80-8 (E)-1-[(E)-4-Ethoxynon-2-enylidene]-2-[4-(trifluoromethyl)phenyl]- 
• 1402134-70-6 6-pentyl-1-[3-(trifluoromethyl)phenyl]-1,6-dihydropyridazine 
• 1402134-69-3 (1E,2E)-1-[2-(perfluorophenyl)hydrazono]non-2-en-4-ol 
• 1402134-68-2 (1E,2E)-1-{2-[2,4-bis(trifluoromethyl)phenyl]hydrazono}non-2-en-4-ol 

Relevant articles and documents

Ordered Porous Pd Octahedra Covered with Monolayer Ru Atoms

Monolayer Ru atoms covered highly ordered porous Pd octahedra have been synthesized via the underpotential deposition and thermodynamic control. Shape evolution from concave nanocube to octahedron with six hollow cavities was observed. Using aberration-corrected high-resolution transmission electron microscopy and X-ray photoelectron spectroscopy, we provide quantitative evidence to prove that only a monolayer of Ru atoms was deposited on the surface of porous Pd octahedra. The as-prepared monolayer Ru atoms covered Pd nanostructures exhibited excellent catalytic property in terms of semihydrogenation of alkynes.

Ir-Catalyzed Remote Functionalization by the Combination of Deconjugative Chain-Walking and C-H Activation Using a Transient Directing Group

An Ir-catalyzed reaction of N-benzylideneanilines with functionalized alkenes such as α,β-unsaturated esters gave ortho-substituted benzaldehyde derivatives with a functional group at the remote position after acidic treatment. The present transformation

CYCLOALKYL-CONTAINING CARBOXYLIC ACIDS AND USES THEREOF

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Electrophilic Iron Catalyst Paired with a Lithium Cation Enables Selective Functionalization of Non-Activated Aliphatic C?H Bonds via Metallocarbene Intermediates

Combining an electrophilic iron complex [Fe(Fpda)(THF)]2 (3) [Fpda=N,N′-bis(pentafluorophenyl)-o-phenylenediamide] with the pre-activation of α-alkyl-substituted α-diazoesters reagents by LiAl(ORF)4 [ORF=(OC(CF3)3] provides unprecedented access to selective iron-catalyzed intramolecular functionalization of strong alkyl C(sp3)?H bonds. Reactions occur at 25 °C via α-alkyl-metallocarbene intermediates, and with activity/selectivity levels similar to those of rhodium carboxylate catalysts. Mechanistic investigations reveal a crucial role of the lithium cation in the rate-determining formation of the electrophilic iron-carbene intermediate, which then proceeds by concerted insertion into the C?H bond.