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Acetic acid 2-methyl-4-penten-2-yl ester, also known as 2-methyl-4-penten-2-yl acetate, is a chemical compound with the molecular formula C7H12O2. It is an ester derived from acetic acid and 2-methyl-4-penten-2-ol, featuring a fruity, apple-like aroma. This colorless liquid is commonly used as a flavoring agent in the food and beverage industry, as well as in the production of fragrances and cosmetics. It is known for its ability to impart a fresh, green, and fruity scent, making it a popular choice for enhancing the aroma of various products. The compound is typically synthesized through the esterification of acetic acid with 2-methyl-4-penten-2-ol, and its safety and environmental impact are considered when used in commercial applications.

926-22-7

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926-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 926-22-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 926-22:
(5*9)+(4*2)+(3*6)+(2*2)+(1*2)=77
77 % 10 = 7
So 926-22-7 is a valid CAS Registry Number.

926-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylpent-4-en-2-yl acetate

1.2 Other means of identification

Product number -
Other names Acetat v. 4-Methylpent-1-en-4-ol

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:926-22-7 SDS

926-22-7Relevant academic research and scientific papers

Remote Arylative Substitution of Alkenes Possessing an Acetoxy Group via β-Acetoxy Elimination

Kakiuchi, Fumitoshi,Kochi, Takuya,Kumagai, Takaaki,Muto, Kazuma

supporting information, p. 24500 - 24504 (2021/10/19)

Palladium-catalyzed remote arylative substitution was achieved for the reaction of arylboronic acids with alkenes possessing a distant acetoxy group to provide arylation products having an alkene moiety at the remote position. The use of β-acetoxy elimination as a key step in the catalytic cycle allowed for regioselective formation of unstabilized alkenes after chain walking. This reaction was applicable to various arylboronic acids as well as alkene substrates.

Kinetic Applications of Electron Paramagnetic Resonance Spectroscopy. 38. Rearrangement of β-(Acyloxy)alkyl and β-(benzoyloxy)alkyl Radicals

Barclay, L. R. C.,Griller, D.,Ingold, K. U.

, p. 4399 - 4403 (2007/10/02)

Rate constants for the free-radical rearrangement, RC(O)OCMe2CH2* --> RC(O)OCH2CMe2*, and for the ring-opening reaction, , have been measured by kinetic EPR spectroscopy.In hydrocarbon solvents at 75 deg C with R = methyl and phenyl, the 1,2-acy

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