25118-23-4

Basic information

• Product Name: ETHYL 6-HEPTENOATE 98
• Synonyms: ETHYL 6-HEPTENOATE 98;6-Heptenoic acid ethyl ester;Ethyl 6-heptenoate 98%;Ethylhept-6-enoate97%
• CAS NO: 25118-23-4
• Molecular Formula: C₉H₁₆O₂
• Molecular Weight: 156.22
• Product Categories: C8 to C9;Carbonyl Compounds;Esters;Building Blocks;C8 to C9;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks
• Mol File: 25118-23-4.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 189 °C(lit.)
• Flash Point: 175 °F
• Appearance: /
• Density: 0.89 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.576mmHg at 25°C
• Refractive Index: n20/D 1.426(lit.)
• CAS DataBase Reference: ETHYL 6-HEPTENOATE 98(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 6-HEPTENOATE 98(25118-23-4)
• EPA Substance Registry System: ETHYL 6-HEPTENOATE 98(25118-23-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 25118-23-4(Hazardous Substances Data)

Usage

General Description

ETHYL 6-HEPTENOATE 98 is a chemical compound with a formula C9H16O2. It is also known as ethyl trans-6-heptenoate and is commonly used as a flavoring agent in the food and beverage industry, providing a fruity, pineapple-like aroma. It is also used in the fragrance industry to create scents with a fruity, tropical character. This chemical is a colorless to pale yellow liquid with a fruity odor and is stable under normal temperatures and pressures. It is important to handle it with care and follow safety precautions due to its volatile nature and potential irritant properties. Overall, ETHYL 6-HEPTENOATE 98 is a versatile chemical widely used in the flavor and fragrance industry for its pleasant fruity aroma.

InChI:InChI=1/C9H16O2/c1-3-5-6-7-8-9(10)11-4-2/h3H,1,4-8H2,2H3

Upstream product

• 26040-65-3 ethyl 7-chloroheptanoate 
• 140-89-6 potassium ethyl xanthogenate 
• 34762-21-5 (2,6-Bis-ethoxycarbonyl-hexyl)-triphenyl-phosphonium; bromide 
• 2969-81-5 Ethyl 4-bromobutyrate 
• 106-95-6 allyl bromide 
• 5162-44-7 1-bromo-4-butene 
• 140-88-5 ethyl acrylate 
• 64-17-5 ethanol 
• 288400-62-4 ethyl 2-(pyrimidin-2-ylsulfonyl)hept-6-enoate 
• 1119-51-3 bromopentene 
• 33574-02-6 cyclopropylmethyl iodide 
• 193065-68-8 (3-ethoxy-3-oxopropyl)zinc(II) bromide 
• 1292288-79-9 diethyl 1-chlorohex-5-ene-1,1-dicarboxylate 
• 1292288-80-2 ethyl 2-chlorohept-6-enoate 

Downstream Products

• 663613-17-0 1-benzenesulfonyloct-7-en-2-one 
• 106-30-9 ethyl heptanoate 
• 361353-73-3 2-pent-4-enyl-succinic acid diethyl ester 
• 114578-44-8 hept-6-enoylhydrazone 
• 6149-48-0 ethyl 7-hydroxyheptanoate 
• 34997-46-1 heptanoate d'isopropyle 
• 1220520-29-5 (E)-ethyl 7-[4-[bicyclo[3.3.1]non-9-ylidene(4-hydroxyphenyl)methyl]phenyl]hept-6-enoate 
• 1070-64-0 6,8-dichlorooctanoic acid ethyl ester 
• 133398-13-7 (R)-10-methyloctadecanoic acid 
• 1082670-89-0 ethyl (R)-10-methyloctadecanoate 
• 927888-76-4 (S)-10-methyloctadecanoic acid 
• 57289-48-2 (+)(S)-10-methyl-stearic acid ethyl ester 

Relevant articles and documents

α-Ethoxycarbonyl and α-methoxy substituted radical clocks

Rate constants and Arrhenius functions for 5-exo cyclizations of the 1-(ethoxycarbonyl)-5-hexenyl radical, the 1-(ethoxycarbonyl)-1-methyl-5-hexenyl radical and the 1-methoxy-5-hexenyl radical were determined by indirect kinetic methods.

Cyclization Reactions of Oxyallyl Cation. A Method for Cyclopentane Ring Formation

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An efficient method for the direct allylation of alkyl halides catalyzed by simple cobalt(II) bromide has been developed. This reaction, using a variety of substituted allylic acetates or carbonates, provides the linear product as the major product. It displays broad substrate scope and good functional group tolerance. Copyright