50373-10-9 Usage
Description
(1R)-TROP-2-ENE-2-CARBOXYLIC ACID METHYL ESTER, also known as trop-2-ene-2-carboxylic acid methyl ester, is a chemical compound that belongs to the class of esters. It is derived from trop-2-ene-2-carboxylic acid, which is a bicyclic organic compound. (1R)-TROP-2-ENE-2-CARBOXYLIC ACID METHYL ESTER is characterized by its unique structure and properties, making it a versatile building block in the field of organic chemistry.
Uses
Used in Pharmaceutical Industry:
(1R)-TROP-2-ENE-2-CARBOXYLIC ACID METHYL ESTER is used as an intermediate for the synthesis of various drugs and fine chemicals. Its unique structure and properties make it a valuable component in the development of new pharmaceuticals, contributing to the advancement of medicine and healthcare.
Used in Agrochemical Industry:
(1R)-TROP-2-ENE-2-CARBOXYLIC ACID METHYL ESTER is also used as a building block for the production of various agrochemicals. Its versatility allows it to be incorporated into the development of new compounds that can improve agricultural practices and contribute to sustainable food production.
Used in Organic Synthesis:
(1R)-TROP-2-ENE-2-CARBOXYLIC ACID METHYL ESTER is used as a key component in the preparation of a wide range of organic compounds. Its unique structure allows it to be easily modified and combined with other compounds, making it an essential tool for chemists in the field of organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 50373-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,7 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 50373-10:
(7*5)+(6*0)+(5*3)+(4*7)+(3*3)+(2*1)+(1*0)=89
89 % 10 = 9
So 50373-10-9 is a valid CAS Registry Number.
50373-10-9Relevant articles and documents
METHOD FOR THE PREPARATION OF N-MONOFLUOROALKYL TROPANES AND THEIR USE
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Page/Page column 15, (2021/07/31)
The present invention relates to a method for the preparation of an N-monofluoroalkyl tropane, a method for the preparation of a trialkyltin tropane, a method for the preparation of an iodinated and/or radioiodinated tropane and the use of the N-monofluoroalkyl tropane as a precursor in the method for the preparation of the trialkyltin tropane and/or the iodinated and/or radioiodinated tropane.
Synthesis of 3-arylecgonine analogues as inhibitors of cocaine binding and dopamine uptake
Kline Jr.,Wright,Fox,Eldefrawi
, p. 2024 - 2027 (2007/10/02)
3-Arylecgonine analogues were synthesized and characterized by 1H and 13C NMR, IR, and MS. The compounds were synthesized as racemates from cycloheptatriene-7-carboxylic acid or enantiomerically from (-)-cocaine. These analogues were tested for their ability to inhibit [3H]cocaine binding to bovine striatal tissue and to inhibit [3H]dopamine uptake into striatal synaptosomes. Methyl (1RS-2-exo-3-exo)-8-methyl-3-phenyl-8-azabicyclo[3.2.1]octane-2-carboxylate was the most potent analogue. IC50 values for inhibition of cocaine binding and dopamine uptake were 20 and 100 nM, respectively. The racemates and the 1R isomers were equally potent inhibitors of binding and uptake. Methyl (1RS-2-endo-3-exo)-3-(2,4-dinitrophenyl)-8-methyl-8- azabicyclo[3.2.1]octane-2-carboxylate was the least potent. IC50 for inhibition of both binding and uptake was 40 μM.