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Methyl 5-methyl-2,4-dioxohexanoate is a chemical compound with the molecular formula C8H12O4. It is a methyl ester of 5-methyl-2,4-dioxohexanoic acid and is characterized by its clear, colorless liquid form and fruity odor.

20577-64-4

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20577-64-4 Usage

Uses

Used in Food Industry:
Methyl 5-methyl-2,4-dioxohexanoate is used as a flavoring ingredient for its distinctive fruity aroma, enhancing the taste and appeal of various food products.
Used in Pharmaceutical Industry:
Methyl 5-methyl-2,4-dioxohexanoate serves as a key component in the synthesis of several pharmaceuticals, contributing to the development of new medications and therapies.
Used in Cosmetic Industry:
In the cosmetic industry, methyl 5-methyl-2,4-dioxohexanoate is utilized in the production of perfumes and fragrances, adding a pleasant scent to various cosmetic products.
Additionally, it can be employed as a solvent or reagent in organic synthesis, further expanding its applications across different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 20577-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,7 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20577-64:
(7*2)+(6*0)+(5*5)+(4*7)+(3*7)+(2*6)+(1*4)=104
104 % 10 = 4
So 20577-64-4 is a valid CAS Registry Number.

20577-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 5-methyl-2,4-dioxohexanoate

1.2 Other means of identification

Product number -
Other names methyl 2,4-dioxo-5-methylhexenoate

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:20577-64-4 SDS

20577-64-4Relevant academic research and scientific papers

Synthesis, Acaricidal Activity, and Structure-Activity Relationships of Pyrazolyl Acrylonitrile Derivatives

Yu, Haibo,Cheng, Yan,Xu, Man,Song, Yuquan,Luo, Yanmei,Li, Bin

, p. 9586 - 9591 (2017/01/12)

A series of novel pyrazolyl acrylonitrile derivatives was designed, targeting Tetranychus cinnabarinus, and synthesized. Their structures were identified by combination of1H NMR,13C NMR, and MS spectra. The structures of compounds 18 and 19 were further confirmed by X-ray diffraction. Extensive greenhouse bioassays indicated that compound 19 exhibits excellent acaricidal activity against all developmental stages of T. cinnabarinus, which is better than the commercialized compounds cyenopyrafen and spirodiclofen. It was shown that the acute toxicity of compounds 19 to mammals is quite low. The structure-activity relationships are also discussed.

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