2482-39-5

Basic information

• Product Name: METHYL T2 DECENOATE
• Synonyms: Methyl (2E)-2-decenoate;Methyl 2-decenoate;Methyl ester of 2-Decenoic acid;METHYL TRANS-2-DECENOATE;METHYL T2 DECENOATE;RARECHEM AL BF 0226;2-Decenoic acid, methyl ester;METHYLDEC-2-ENOATE
• CAS NO: 2482-39-5
• Molecular Formula: C₁₁H₂₀O₂
• Molecular Weight: 184.28
• EINECS: 219-618-9
• Mol File: 2482-39-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 235.7 °C at 760 mmHg
• Flash Point: 106.1 °C
• Appearance: /
• Density: 0.889g/cm³
• Vapor Pressure: 0.0495mmHg at 25°C
• Refractive Index: 1.442
• CAS DataBase Reference: METHYL T2 DECENOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL T2 DECENOATE(2482-39-5)
• EPA Substance Registry System: METHYL T2 DECENOATE(2482-39-5)

Safety Data

• Hazardous Substances Data: 2482-39-5(Hazardous Substances Data)

Usage

General Description

Methyl T2 decenoate is a chemical compound belonging to the methyl ester family. It is commonly used as a flavoring agent and aroma compound in the food and beverage industry. It has a fruity and floral scent with a slightly fatty undertone, making it a popular choice for perfumes, soaps, and other cosmetic products. Methyl T2 decenoate is also used in the manufacturing of pharmaceuticals and as an intermediate in organic synthesis. Additionally, it has potential applications in the agricultural and pest control sectors. Overall, Methyl T2 decenoate is a versatile chemical with various industrial uses.

InChI:InChI=1/C11H20O2/c1-3-4-5-6-7-8-9-10-11(12)13-2/h9-10H,3-8H2,1-2H3

Upstream product

• 124-13-0 Octanal 
• 21204-67-1 methyl (triphenylphosphoranylidene)acetate 
• 5927-18-4 trimethyl phosphonoacetate 
• 191018-97-0 methyl bis(4-fluorophenyl)phosphonoacetate 
• 273201-08-4 methyl bis(4-bromophenyl)phosphonoacetate 
• 273201-07-3 methyl bis(4-chlorophenyl)phosphonoacetate 
• 273201-12-0 methyl bis(2,6-xylyl)phosphonoacetate 
• 273201-09-5 methyl bis(4-iodophenyl)phosphonoacetate 
• 273201-11-9 methyl bis(2,6-dichlorophenyl)phosphonoacetate 
• 273201-10-8 methyl bis(2,6-difluorophenyl)phosphonoacetate 

Downstream Products

• 1236003-35-2 methyl (S,S)-3-[N-tert-butyldimethylsilyloxy-N-(α-methylbenzyl)amino]decanoate 
• 7011-82-7 methyl 4-oxodecanoate 
• 139573-87-8 (+/-)-methyl-3-benzyloxydecanoate 

Relevant articles and documents

Water is an efficient medium for Wittig reactions employing stabilized ylides and aldehydes

Water is demonstrated to be an excellent medium for the Wittig reaction employing stabilized ylides and aldehydes. Although the solubility in water appears to be an unimportant characteristic in achieving good chemical yields and E/Z-ratios, the rate of W

A study on the Z-selective Horner-Wadsworth-Emmons (HWE) reaction of methyl diarylphosphonoacetates

Experimental and theoretical studies were conducted to explore the Z-selectivities in the Horner-Wadsworth-Emmons (HWE) reaction employing several methyl diarylphosphonoacetates (3, 4, 5 and 6) and aldehydes. The Z-selectivity depended upon the reaction conditions such as the bases, reaction temperature, and the aromatic substituents on the phosphorus atoms but the almost phosphonoacetates used in the present study showed Z-selectivity in the reactions with both aromatic and aliphatic aldehydes. While the phosphonoacetate (3) with bis(2,4-difluorophenyl)phosphono group showed the highest Z-selectivity in all reaction conditions employed, decrease of the selectivity was observed in the case of some phosphonoacetates with diarylphosphono groups. These experimental results and the theoretical studies calculated by AM1 or 3-21G* ab initio methods suggested that the steric effect in the transition states of the addition steps was important rather than the electronic effect. A different aspect of the reaction courses between the Wittig and HWE reactions in the present computational chemistry was also described.