894789-84-5 Usage
Chemical class
Carboxylic acids
Explanation
Different sources of media describe the Explanation of 894789-84-5 differently. You can refer to the following data:
1. It is a compound containing a functional group composed of a carbon atom double-bonded to an oxygen atom and single-bonded to a hydroxyl group.
2. It is derived from a bicyclic compound containing a tetrahydropyran ring and a methyl group.
3. The compound has a tetrahydropyran ring, which is a six-membered oxygen-containing heterocycle, forming a bicyclic structure.
4. The compound contains a methyl group (CH3) attached to the tetrahydro-2H-pyran ring, contributing to its structure and properties.
5. 2-(4-Methyl-tetrahydro-2H-pyran-4-yl)acetic acid may have applications in pharmaceutical, agricultural, or industrial fields due to its unique structure and properties.
6. The compound could be used for the synthesis of more complex molecules or as a starting material for the production of other chemicals, requiring further research and testing to understand its full potential.
Check Digit Verification of cas no
The CAS Registry Mumber 894789-84-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,4,7,8 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 894789-84:
(8*8)+(7*9)+(6*4)+(5*7)+(4*8)+(3*9)+(2*8)+(1*4)=265
265 % 10 = 5
So 894789-84-5 is a valid CAS Registry Number.
894789-84-5Relevant articles and documents
Ligand-Enabled γ-C(sp3)?H Olefination of Free Carboxylic Acids
Ghiringhelli, Francesca,Ghosh, Kiron Kumar,Mondal, Arup,Uttry, Alexander,Wedi, Philipp,van Gemmeren, Manuel
supporting information, p. 12848 - 12852 (2020/06/25)
We report the ligand-enabled C?H activation/olefination of free carboxylic acids in the γ-position. Through an intramolecular Michael addition, δ-lactones are obtained as products. Two distinct ligand classes are identified that enable the challenging palladium-catalyzed activation of free carboxylic acids in the γ-position. The developed protocol features a wide range of acid substrates and olefin reaction partners and is shown to be applicable on a preparatively useful scale. Insights into the underlying reaction mechanism obtained through kinetic studies are reported.
AMIDO SPIROCYCLIC AMIDE AND SULFONAMIDE DERIVATIVES
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Page/Page column 181; 182, (2013/09/12)
Provided are amido spirocyclic amide and sulfonamide compounds, pharmaceutical compositions comprising such compounds, and methods of treatment using such compounds.
INHIBITORS OF SERINE PROTEASES FOR THE TREATMENT OF HCV INFECTIONS
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Page/Page column 471, (2008/12/07)
The present invention relates to compounds of formula (I): or a pharmaceutically acceptable salt thereof. These compounds inhibit serine protease, particularly the hepatitis C virus NS3-NS4A protease.