76650-25-4 Usage
Chemical class
Organic compound, specifically a phenylpropanoic acid.
Explanation
It is a type of organic compound that belongs to the phenylpropanoic acids class.
Explanation
It has the ability to reduce inflammation, which is a key characteristic of this chemical compound.
Explanation
It is part of a family of chemical compounds that share a similar structure and properties.
Explanation
The compound consists of a propionic acid subunit that has been modified.
Explanation
The propionic acid subunit is substituted at the 2-position with a specific functional group, which influences the compound's properties and activity.
Explanation
It is commonly used to reduce pain, inflammation, and fever, similar to other NSAIDs.
Explanation
2-(2'-Methoxy-5'-methylphenyl)-propanoic acid is also known by the more familiar name, ibuprofen.
Explanation
It is widely accessible in medications that are designed to provide relief from pain without the need for a prescription.
Functionality
Anti-inflammatory agent.
Family
2-arylpropionic acids.
Structural feature
Propionic acid derivative.
Substitution
2-position with a 2'-methoxy-5'-methylphenyl group.
Common use
Non-steroidal anti-inflammatory drug (NSAID).
Availability
Found in over-the-counter medications for pain relief.
Check Digit Verification of cas no
The CAS Registry Mumber 76650-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,5 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76650-25:
(7*7)+(6*6)+(5*6)+(4*5)+(3*0)+(2*2)+(1*5)=144
144 % 10 = 4
So 76650-25-4 is a valid CAS Registry Number.
76650-25-4Relevant articles and documents
Thermal Rearrangement of 2-Methyl-2-(2'-acetoxy-5'-methylphenyl)oxirane
Dhekne, Vijay V.,Rao, A. S.
, p. 852 - 855 (2007/10/02)
Thermal rearrangement of 2-methyl-(2'-acetoxy-5'-methylphenyl)oxirane (2) at 160 deg C for 1 hr furnishes a mixture of 2-(2'-hydroxy-5'-methylphenyl)propenyl acetate (4), 3,5-dimethylbenzofuran (11), 2-(2'-acetoxy-5'-methylphenyl)-propenyl acetate (5), 2-hydroxy-5-methylacetophenone (13), (+/-)-2,3-dihydro-3α,5-dimethylbenzofuran-2β-ol (14) and (+/-)-2,3-dihydro-3β,5-dimethylbenzofuran-2β-ol (15).Evidences in support of E-geometry at the ethylenic linkage of enolester (4) are presented.Treatment of 4 with alkali in the presence of air furnishes 13.Oxidation of a mixture of 14 and 15 gives 2,3-dihydro-3,5-dimethylbenzofuran-2-one (19). 3,5-Dimethylbenzofuran (11) has been prepared from 4.Thermal rearrangement of 2-methyl-(2'-acetoxy-5'-bromophenyl)oxirane (27) furnishes 5-bromo-3-methylbenzofuran (12) in good yield.
