15876-37-6 Usage
Description
(2E)-octahydronaphthalen-2(1H)-one oxime, also known as 2-oxime-2-hydronaphthalene, is a white crystalline chemical compound with the molecular formula C10H13NO. It is an oxime derivative of octahydronaphthalen-2(1H)-one and is soluble in organic solvents such as ethanol, acetone, and ether. (2E)-octahydronaphthalen-2(1H)-one oxime has potential applications in the field of organic chemistry and pharmaceuticals, and its properties make it a useful building block for the creation of more complex molecules. Additionally, it is known to have mild stimulant properties and has been studied as a potential treatment for neurological disorders.
Uses
Used in Organic Chemistry:
(2E)-octahydronaphthalen-2(1H)-one oxime is used as a building block for the synthesis of more complex organic compounds due to its unique structure and reactivity.
Used in Pharmaceutical Industry:
(2E)-octahydronaphthalen-2(1H)-one oxime is used as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Neurological Disorders Research:
(2E)-octahydronaphthalen-2(1H)-one oxime is used as a potential treatment for neurological disorders due to its mild stimulant properties, and it is being studied for its potential therapeutic effects.
Check Digit Verification of cas no
The CAS Registry Mumber 15876-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,7 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15876-37:
(7*1)+(6*5)+(5*8)+(4*7)+(3*6)+(2*3)+(1*7)=136
136 % 10 = 6
So 15876-37-6 is a valid CAS Registry Number.
15876-37-6Relevant articles and documents
Reactivite nucleophile des cyclanones: influence de la stereochimie cis/trans en serie bicyclique
Agami, C.,Rizk, T.,Durand, R.,Geneste, P.
, p. 2355 - 2357 (2007/10/02)
The relative reactivities of a number of cis/trans pairs of bicyclic ketones in the 1- and 2-decalone series (2-decalone; 10-methyl-2-decalone; 9-methyl-1-decalone; and 3,10-dimethyl-2-decalone) have been studied for the nucleophilic addition of hydroxylamine in acidic medium.The results obtained as well as the rate constants for neutral or acid catalysed addition always reveal a slight preference for the trans-isomer (x 2.4).This result agrees with the proposal that preferential equatorial attack of a nucleophile is caused by conformational factors related to a steroid non-steroid conformation equilibrium in the cis-isomers.