4488-40-8 Usage
Description
4-Methyl-1-naphthoic acid is a naphthoic acid derivative, which is an organic compound belonging to the class of naphthalene-based carboxylic acids. It is characterized by its off-white solid appearance and is known for its potential applications in various chemical and pharmaceutical processes.
Uses
1. Chemical Synthesis:
4-Methyl-1-naphthoic acid is used as a key intermediate in the synthesis of various organic compounds, including:
2-methyl-1-propyl-3-(4-methyl-1-naphthoyl)indole
JWH-148
4-methyl-1-naphthylcarbinol1,4-dioxan-2-yl 4-methyl-1-naphthoate
2. Agricultural Applications:
In the agricultural industry, 4-Methyl-1-naphthoic acid is used as an antidote for urea and other herbicides. Its application helps mitigate the negative effects of these herbicides on crops and the environment.
3. Pharmaceutical Applications:
Although not explicitly mentioned in the provided materials, given its chemical structure and potential for synthesis, 4-Methyl-1-naphthoic acid may also find applications in the pharmaceutical industry, possibly as a precursor for the development of new drugs or drug candidates with various therapeutic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 4488-40-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,8 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4488-40:
(6*4)+(5*4)+(4*8)+(3*8)+(2*4)+(1*0)=108
108 % 10 = 8
So 4488-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H10O2/c1-8-6-7-11(12(13)14)10-5-3-2-4-9(8)10/h2-7H,1H3,(H,13,14)
4488-40-8Relevant articles and documents
Redox-Neutral Photocatalytic C?H Carboxylation of Arenes and Styrenes with CO2
Bergonzini, Giulia,Brandt, Peter,Fricke, Florian,Johansson, Magnus J.,K?nig, Burkhard,Schmalzbauer, Matthias,Svejstrup, Thomas D.
supporting information, p. 2658 - 2672 (2020/10/07)
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Aryllithiums with increasing steric crowding and lipophilicity prepared from chlorides in diethyl ether. the first directly prepared room-temperature-stable dilithioarenes
Screttas, Constantinos G.,Steele, Barry R.,Micha-Screttas, Maria,Heropoulos, Georgios A.
supporting information, p. 5680 - 5683 (2013/01/15)
A convenient procedure has been developed for the preparation of synthetically useful, room-temperature-stable aryllithiums starting from aryl chlorides and lithium metal. The method provides a route to aryllithiums which have previously not been accessible cleanly or could only be prepared by using more expensive starting materials.
HYDROXYCARBONYLATION OF ARYL AND VINYL BROMIDES
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Page/Page column 10; 12; 13; 15, (2008/06/13)
Process for the preparation of aryl or vinyl carboxylic acids via Pd-catalysed hydroxycarbonylation of aryl and vinyl bromides, wherein the aryl or vinyl bromides are reacted with a carbon monoxide source comprising lithium formate and acetic acid anhydride, in the presence of the combination of palladium complexes with the chelating ligand dppf (1,1-bis[diphenylphosphino]ferrocene).
