3238-50-4 Usage
Description
1-Ethyl-7-Methoxy-2-tetralone is a chemical compound with the molecular formula C13H16O2. It is a substituted tetralone, a type of organic compound that contains a six-membered aromatic ring fused to a five-membered ring with a ketone functional group. 1-Ethyl-7-Methoxy-2-tetralone is classified as a ketone and possesses an ethyl and a methoxy group attached to the carbon atoms in the 1 and 7 positions, respectively.
Used in Organic Chemistry:
1-Ethyl-7-Methoxy-2-tetralone is used as a synthetic intermediate for the production of various organic compounds.
Used in Pharmaceutical Research:
1-Ethyl-7-Methoxy-2-tetralone is used as a building block in the development of new pharmaceuticals.
Used in Biological Activities and Pharmacological Properties Research:
1-Ethyl-7-Methoxy-2-tetralone is used as a subject of study for its potential biological activities and pharmacological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 3238-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,3 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3238-50:
(6*3)+(5*2)+(4*3)+(3*8)+(2*5)+(1*0)=74
74 % 10 = 4
So 3238-50-4 is a valid CAS Registry Number.
3238-50-4Relevant articles and documents
Benzobicycloalkane ketones
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, (2008/06/13)
Benzobicycloalkane amines, their pharmacologically acceptable addition salts, intermediates therefore the processes for their preparation and use. The compounds of the invention exert analgesic and anti-inflammatory activity.
9-Alkoxy-5-methyl-6,7-benzomorphans
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, (2008/06/13)
N-Substituted-9-alkoxy-5-methyl-6,7-benzomorphans have been found to possess potent narcotic agonist and/or antagonist activity. In particular, the compound 2-cyclopropylmethyl-2'-hydroxy-9α-methoxy-5-methyl-6,7-benzomorphan has been found to possess potent narcotic agonist and antagonist activity. These compounds are prepared by total synthesis and are not derived from opium alkaloids.