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3-Pentenoic acid ethyl ester, also known as ethyl 3-pentenoate, is an organic compound with the chemical formula C7H12O2. It is a colorless liquid with a fruity, apple-like odor. This ester is formed by the reaction of 3-pentenoic acid and ethanol, and it is commonly used as a flavoring agent and fragrance compound in the food and perfume industries. It is also utilized as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals. 3-Pentenoic acid ethyl ester is characterized by its molecular weight of 128.17 g/mol, a boiling point of 140-142°C, and a density of approximately 0.91 g/cm3. It is insoluble in water but soluble in most organic solvents.

1617-05-6

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1617-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1617-05-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1617-05:
(6*1)+(5*6)+(4*1)+(3*7)+(2*0)+(1*5)=66
66 % 10 = 6
So 1617-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c1-3-5-6-7(8)9-4-2/h3,5H,4,6H2,1-2H3

1617-05-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl pent-3-enoate

1.2 Other means of identification

Product number -
Other names ethyl-3-pentenoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1617-05-6 SDS

1617-05-6Downstream Products

1617-05-6Relevant articles and documents

New generation biofuels: γ-Valerolactone into valeric esters in one pot

Chan-Thaw, Carine E.,Marelli, Marcello,Psaro, Rinaldo,Ravasio, Nicoletta,Zaccheria, Federica

, p. 1302 - 1306 (2013)

Ethyl valerate and pentyl valerate, suitable as a gasoline additive and diesel component respectively, can be obtained in a one pot one step reaction from γ-valerolactone, readily available from lignocellulosic biomass. The reaction takes place in ethanol under H2 through nucleophilic addition of the alcohol to the carboxylic group giving hydroxypentanoate, dehydration to pentenoate and hydrogenation to the saturated ester. The bifunctional catalyst used consists of a non noble metal, namely copper, supported on an amorphous weakly acidic material, therefore representing an interesting alternative to Pt-zeolite catalysts. Pentyl valerate can be obtained in one pot with conversions >90% and selectivity up to 83%.

Hydrogenation of γ-valerolactone in ethanol over Pd nanoparticles supported on sulfonic acid functionalized MIL-101

Zhang, Damin,Ye, Feiyang,Guan, Yejun,Wang, Yimeng,Hensen, Emiel J. M.

, p. 39558 - 39564 (2014)

A ligand-based solid solution approach is employed to incorporate sulphonic acid functional groups into the porous coordination polymer Cr-MIL-101. Loaded with Pd nanoparticles these Pd/MIL-101-SO3H materials act as bifunctional catalysts for the one-pot conversion of γ-valerolactone into ethyl valerate (up to 83% yield). The catalysts were extensively characterized before and after reaction. The influence of the sulfonic acid group density and the reaction conditions on the catalytic activity was systematically investigated and the reaction network for γ-valerolactone upgrading was discussed.

Stabilization of cobalt catalysts by embedment for efficient production of valeric biofuel

Sun, Peng,Gao, Guang,Zhao, Zelun,Xia, Chungu,Li, Fuwei

, p. 4136 - 4142 (2015/02/19)

We herein report, for the first time, a bifunctional base-metal catalyst (Co@HZSM-5) that acts as an efficient alternative to noble-metal catalysts (e.g., Pt, Ru) for the conversion of levulinic acid into valeric biofuel under batch and fixed-bed reactor conditions. The cobalt nanoparticles were embedded in HZSM-5 crystals and catalyzed the sequential hydrogenations of the ketone and alkene functional groups; meanwhile, the acidic zeolite catalyzed the ring opening of the γ-valerolactone intermediate. Although base metals (e.g., Co) are abundant and inexpensive, their sintering and/or leaching under liquid-phase conditions always lead to the irreversible deactivation of the catalyst. In this system, the embedment structure stabilizes the nanoparticles, and Co@HZSM-5 could be used up to eight times. This work provides a practical clue toward the stabilization of base-metal catalysts and will inspire the development of large-scale biorefinery.

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