145526-82-5 Usage
Carboxylic acid derivative
It is a compound derived from a carboxylic acid, which is an organic compound containing a carboxyl group (-COOH).
Benzene ring
The compound contains a benzene ring, which is a six-membered aromatic ring consisting of six carbon atoms bonded together through alternating single and double bonds.
Methyl group attachment
A methyl group (-CH3) is attached to the benzene ring, contributing to the compound's structure and properties.
Allyloxy group attachment
An allyloxy group (-OCH2CH=CH2) is also attached to the benzene ring, further modifying the compound's structure and properties.
Usage in pharmaceuticals
2-(allyloxy)-3-methylbenzoic acid is used as a building block for the synthesis of other organic compounds in drug development.
Usage in agrochemicals
The compound is employed in the manufacturing of herbicides and pesticides, contributing to its application in agriculture.
Potential applications in chemical research and development
Due to its unique structure and reactivity, 2-(allyloxy)-3-methylbenzoic acid may have further uses in the field of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 145526-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,5,2 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 145526-82:
(8*1)+(7*4)+(6*5)+(5*5)+(4*2)+(3*6)+(2*8)+(1*2)=135
135 % 10 = 5
So 145526-82-5 is a valid CAS Registry Number.
145526-82-5Relevant articles and documents
Total Synthesis of Ajudazol A by a Modular Oxazole Diversification Strategy
Essig, Sebastian,G?lz, Jan Philipp,Menche, Dirk,Von Schwarzenberg, Karin,Wollnitzke, Philipp
, (2020/09/02)
The total synthesis of the potent respiratory chain inhibitor ajudazol A was accomplished by a concise strategy in 17 steps (longest linear sequence). The modular approach was based on a direct oxazole functionalization strategy involving a halogen dance
Stereoselective Synthesis of Isochromanones by an Asymmetric Ortho-Lithiation Strategy: Synthetic Access to the Isochromanone Core of the Ajudazols
Essig, Sebastian,Menche, Dirk
, p. 1943 - 1966 (2016/03/15)
Full details on the design, development, and application of a highly stereoselective strategy for the synthesis of isochromanones are reported. The method is based on an asymmetric ortho lithiation with aldehyde electrophiles and utilizes the chiral memor
Full stereochemical determination of ajudazols a and b by bioinformatics gene cluster analysis and total synthesis of ajudazol B by an asymmetric ortholithiation strategy
Essig, Sebastian,Bretzke, Sebastian,Müller, Rolf,Menche, Dirk
, p. 19362 - 19365 (2013/02/21)
The stereochemical determination of the potent respiratory chain inhibitors ajudazols A and B and the total synthesis of ajudazol B are reported. Configurational assignment was exclusively based on biosynthetic gene cluster analysis of both ketoreductase
