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β-Succinimidoethyl-1-methoxy-6-dihydro-3,4-naphtalene is a complex organic chemical compound with the molecular formula C15H15NO3. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, with a succinimide group attached to the β-position and a methoxy group at the 1-position. β-succinimidoethyl-1 methoxy-6 dihydro-3,4 naphtalene is characterized by its unique structure, which features a dihydronaphtalene ring system, indicating the presence of two hydrogen atoms in the ring structure. The compound has potential applications in various chemical synthesis processes, particularly in the formation of polymers and other complex organic molecules. Its specific properties and reactivity make it a valuable intermediate in the development of new materials and pharmaceuticals.

39662-46-9

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39662-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39662-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,6 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39662-46:
(7*3)+(6*9)+(5*6)+(4*6)+(3*2)+(2*4)+(1*6)=149
149 % 10 = 9
So 39662-46-9 is a valid CAS Registry Number.

39662-46-9Downstream Products

39662-46-9Relevant academic research and scientific papers

Diazaestrones and analogs. II. Structural modifications of succinimidoethyldihydroisoquinoline, heterosteroid precursor, to establish structure-analgesic activity relationship

Hocquaux,Viel,Brunaud,et al.

, p. 331 - 338 (2007/10/02)

β-1-(succinimidoethyl)-6,7-dimethoxydihydroisoquinoline having exihibited a stronger analgesic activity than the methylester of 2-methoxy-8,13-diazaestrone, its structure has been systematically modified in view of establishing a relation between structur

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