3913-85-7

Basic information

• Product Name: TRANS-2-DECENOIC ACID
• Synonyms: T2 DECENOIC ACID;RARECHEM AL BK 0166;TRANS-2-DECENOIC ACID;TRANS-2-DECYLENIC ACID;FEMA NUMBER 3913;2-DECENOIC ACID;2-DECYLENIC ACID;(2E)-2-Decenoic acid
• CAS NO: 3913-85-7
• Molecular Formula: C₁₀H₁₈O₂
• Molecular Weight: 170.25
• EINECS: 223-475-8
• Mol File: 3913-85-7.mol
• Article Data: 10

Chemical Properties

• Melting Point: 12°C
• Boiling Point: 290.67°C (estimate)
• Flash Point: 185°C
• Appearance: /
• Density: 0.9280
• Vapor Pressure: 0.00113mmHg at 25°C
• Refractive Index: 1.4616
• CAS DataBase Reference: TRANS-2-DECENOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: TRANS-2-DECENOIC ACID(3913-85-7)
• EPA Substance Registry System: TRANS-2-DECENOIC ACID(3913-85-7)

Safety Data

• Hazardous Substances Data: 3913-85-7(Hazardous Substances Data)

Usage

Definition

ChEBI: A decenoic acid having its double bond in position 2.

Synthesis Reference(s)

Tetrahedron Letters, 28, p. 93, 1987 DOI: 10.1016/S0040-4039(00)95658-2

InChI:InChI=1/C10H18O2/c1-2-3-4-5-6-7-8-9-10(11)12/h8-9H,2-7H2,1H3,(H,11,12)/b9-8-

Upstream product

• 111-71-7 heptanal 
• 79-08-3 bromoacetic acid 
• 112-63-0 Methyl linoleate 
• 3452-09-3 1-nonyne 
• 124-38-9 carbon dioxide 
• 124-13-0 Octanal 
• 141-82-2 malonic acid 
• 61746-55-2 Hept₂CuLi 
• 74-86-2 acetylene 
• 52886-17-6 (Z)-1-iodo-1-nonene 
• 37486-72-9 ethyl 2-decenoate 

Downstream Products

• 30779-95-4 falcarindiol 
• 65892-84-4 heptadeca-1,9c-diene-4,6-diyne-3,8-dione 
• 112-30-1 1-Decanol 

Relevant articles and documents

Compound with cinnamon fragrance as well as preparation method and application thereof

The invention relates to a compound with cinnamon fragrance as well as a preparation method and application thereof. The compound has the following structural formula, wherein the structural formula can be named as 2-decenoic acid-2-(4-methoxy)-phenyl-2-butyl ester. The provided compound has the advantages of obvious cinnamon aroma, rich aroma, lasting aroma and good stability, and enriches the sources of cinnamon aroma. When the essence is prepared in different periods, the compound has consistent cinnamon aroma, so that the required aroma can be accurately mastered.

Enantioselective Synthesis of N?H-Free 1,5-Benzothiazepines

An enantioselective sulfa-Michael-cyclization reaction was developed for the synthesis of 1,5-benzothiazepines with versatile pharmacological activities. The reaction between 2-aminothiophenol and α,β-unsaturated pyrazoleamides gave direct access to N?H-free 1,5-benzothiazepines in the presence of a chiral N,N′-dioxide/Yb(OTf)3complex. Excellent enantioselectivities (up to 96 % ee) and high yields (up to 99 %) were obtained for a broad range of substrates under mild reaction conditions. This method provided a facile approach to the antidepressant drug (R)-(?)-Thiazesim.

A detailed identification study on high-temperature degradation products of oleic and linoleic acid methyl esters by GC-MS and GC-FTIR

GC-MS and GC-FTIR were complementarily applied to identify oxidation compounds formed under frying conditions in methyl oleate and linoleate heated at 180 °C. The study was focused on the compounds that originated through hydroperoxide scission that remain attached to the glyceridic backbone in fats and oils and form part of non-volatile molecules. Twenty-one short-chain esterified compounds, consisting of 8 aldehydes, 3 methyl ketones, 4 primary alcohols, 5 alkanes and 1 furan, were identified. In addition, twenty non-esterified volatile compounds, consisting of alcohols, aldehydes and acids, were also identified as major non-esterified components. Furanoid compounds of 18 carbon atoms formed by a different route were also identified in this study. Overall, the composition of the small fraction originated from hydroperoxide scission provides a clear idea of the complexity of the new compounds formed during thermoxidation and frying.