13481-87-3

Basic information

• Product Name: FEMA 3710
• Synonyms: METHYL 3-NONENOATE;METHYL TRANS-3-NONENOATE;METHYL T3 NONENOATE;FEMA 3710;TRANS-NONENOIC ACID METHYL ESTER;3-Nonenoicacid,methylester;methyltrans-3-nonsenoate;methyl non-3-enoate
• CAS NO: 13481-87-3
• Molecular Formula: C₁₀H₁₈O₂
• Molecular Weight: 170.25
• EINECS: 236-786-9
• Product Categories: Alphabetical Listings;Flavors and Fragrances;M-N
• Mol File: 13481-87-3.mol

Chemical Properties

• Boiling Point: 212.7 °C at 760 mmHg
• Flash Point: 191 °F
• Appearance: /
• Density: 0.885 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.171mmHg at 25°C
• Refractive Index: n20/D 1.436(lit.)
• CAS DataBase Reference: FEMA 3710(CAS DataBase Reference)
• NIST Chemistry Reference: FEMA 3710(13481-87-3)
• EPA Substance Registry System: FEMA 3710(13481-87-3)

Safety Data

• WGK Germany: 2
• Hazardous Substances Data: 13481-87-3(Hazardous Substances Data)

Usage

Uses

Used in Flavor Industry:
FEMA 3710 is used as a flavoring agent for its watermelon-like odor. It is commonly added to various food and beverage products to provide a refreshing and fruity taste.
Used in Fragrance Industry:
FEMA 3710 is used as a fragrance ingredient for its watermelon-like scent. It is often incorporated into personal care products, cleaning supplies, and air fresheners to create a pleasant and natural aroma.

InChI:InChI=1/C10H18O2/c1-3-4-5-6-7-8-9-10(11)12-2/h7-8H,3-6,9H2,1-2H3/b8-7+

Upstream product

• 111-71-7 heptanal 
• 5927-18-4 trimethyl phosphonoacetate 
• 67-56-1 methanol 
• 4124-88-3 3-nonenoic acid 

Downstream Products

• 4124-88-3 3-nonenoic acid 
• 10339-61-4 3-nonene-1-ol 
• 10339-61-4 (E)-non-3-en-1-ol 
• 143-08-8 nonyl alcohol 
• 287483-41-4 (4S,5S)-4-(tert-butyldiphenylsilanyloxy)-5-pentyldihydrofuran-2-one 
• 1422267-58-0 C₂₅H₃₈O₃Si 
• 1422267-50-2 C₃₁H₄₈O₃Si₂ 
• 1422267-52-4 C₃₆H₅₀O₃Si₂ 
• 1422267-54-6 C₂₈H₃₉BrO₃Si 
• 287483-51-6 (1S)-1-[(4S,5S,2S)-4-(tert-butyldiphenylsilanyloxy)-5-pentyltetrahydrofuran-2-yl]-dec-9-en-1-ol 
• 1541181-05-8 (2R,3S)-5,5-dimethyl-2 pentyltetrahydrofuran-3-ol 

Relevant articles and documents

Catalytic Regio- and Enantioselective Oxytrifluoromethylthiolation of Aliphatic Internal Alkenes by Neighboring Group Assistance

Chiral selenide-catalyzed oxytrifluoromethylthiolation of aliphatic internal alkenes by a formally intermolecular strategy is disclosed, affording CF3S 1,3-amino alcohol and 1,3-diol derivatives with high regio-, enantio-, and diastereoselectivities. The reactions are promoted by a neighboring imide or ester group on substrates via a six-membered ring transition state. This assistance strategy is also successfully applied to the regio- and diastereoselective oxyhalofunctionalization of internal alkenes and the conversion of alkynes.

Upgrading castor oil: From heptanal to non-isocyanate poly(amide-hydroxyurethane)s

Intensive research has recently been carried out to synthesize non-isocyanate polyurethanes (NIPUs) from five-membered cyclic carbonates and amines as a sustainable route to industrial relevant polyurethanes. Herein, an activated disubstituted cyclic carbonate and methyl ester containing monomer CE was prepared using castor oil based heptanal and CO2. Good results for the catalytic cycloaddition have been obtained using renewable sugar cane bagasse in combination with TBAB, and this system has been shown to be recyclable. A novel poly(amide-hydroxyurethane) (PAHU) was obtained by bulk ring-opening and amidation polymerization of high reactive CE with 1,6-diaminohexane at low temperature and in absence of catalyst. PAHU contains aliphatic pendant moieties allowing its self-assembling into nanoparticles in aqueous solution, showing potential application in catalysis or drug delivery among other applications.