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5-methyl-2-(propan-2-yl)phenyl 2-methylbutanoate is a complex organic compound with the molecular formula C16H24O2. It is a derivative of phenyl esters, characterized by a phenyl ring with a methyl group at the 5th position and a propyl group at the 2nd position. The molecule is further esterified with 2-methylbutanoic acid, which is a branched-chain carboxylic acid with a methyl group at the 2nd carbon. 5-methyl-2-(propan-2-yl)phenyl 2-methylbutanoate is known for its potential applications in the fragrance industry due to its unique scent profile, and it may also be used as a flavoring agent in food products. The chemical structure and properties of 5-methyl-2-(propan-2-yl)phenyl 2-methylbutanoate make it a versatile compound in the realm of organic chemistry, with potential uses in various industrial applications.

69844-32-2

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69844-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69844-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,4 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69844-32:
(7*6)+(6*9)+(5*8)+(4*4)+(3*4)+(2*3)+(1*2)=172
172 % 10 = 2
So 69844-32-2 is a valid CAS Registry Number.

69844-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-methyl-2-propan-2-ylphenyl) 2-methylbutanoate

1.2 Other means of identification

Product number -
Other names Butanoic acid,2-methyl-,5-methyl-2-(1-methylethyl)phenyl ester

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:69844-32-2 SDS

69844-32-2Relevant academic research and scientific papers

Antinociceptive effect of extracts and compounds from Hofmeisteria schaffneri

Angeles-Lopez, Guadalupe,Perez-Vasquez, Araceli,Hernandez-Luis, Francisco,Deciga-Campos, Myrna,Bye, Robert,Linares, Edelmira,Mata, Rachel

, p. 425 - 432 (2011/11/14)

Ethnopharmacological relevance: Hofmeisteria schaffneri (Asteraceae) is a medicinal plant widely commercialized in the most important Markets of Mexico City for the treatment of gastro-intestinal complaints and skin afflictions. Aim of the study: The main goals of this study were to establish the potential acute toxicity and the antinociceptive activity in animal models of several preparations and compounds from Hofmeisteria schaffneri. Materials and methods: The aqueous and organic extracts as well as the essential oil of Hofmeisteria schaffneri were prepared by infusion, maceration and hydrodistillation, respectively. Investigation of the acute toxicity was accomplished by the Lorke method. The antinociceptive effect was assessed using the writhing and the hot plate tests. Natural compounds were isolated by standard phytochemical procedures. In addition, a few thymol esters were prepared by chemical synthesis. The stability of natural and synthetic esters was qualitatively analyzed by measuring their susceptibility to hydrolysis by pig liver estearase and mouse plasma at 37°C. Results: The LD50 for each preparation tested was higher than 5000mg/kg revealing that they were not toxic to mice after exposure for short space of time. On the other hand, the extracts showed significant antinociceptive effect when tested in the hot plate model. The most active natural product as antinociceptive agent was hofmeisterin III (1) which also was the most stable in the stability study. Its pharmacological effect seems to be partially mediated by an opioid mechanism since naloxone inhibits its action. Using compound 1 as a lead molecule, several synthetic thymol esters were prepared and only compounds 13, 15 and 17 were antinoceptive at the dose of 1mg/kg. Conclusions: The present investigation provided evidence of the efficacy of several preparations of Hofmeisteria schaffneri as antinociceptive agents. The most active preparation was the essential oil which contained large amount of hofmeisterin III (1) and other thymol derivatives. Some novel synthetic analogs of hofmeisterin III with antinociceptive properties were discovered. The nature of the ester chain of these analogs did not have a clear impact on the antinociceptive activity. The phyto-preparations analyzed in this study were not toxic to mice according to the Lorke's test; therefore considering their long term use of the plant they might be secure for human consumption.

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