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5-(benzyloxy)-4-methoxy-2-nitrotoluene is an organic compound characterized by its molecular formula C15H15NO4. 5-(benzyloxy)-4-methoxy-2-nitrotoluene features a toluene core, which is a methyl-substituted benzene, with a nitro group at the 2-position, providing it with explosive properties. The 4-position is occupied by a methoxy group, which is a methyl ether, and the 5-position is substituted with a benzyloxy group, which is a benzyl ether. The presence of these functional groups endows the molecule with specific chemical reactivity and properties. It is important to note that due to the nitro group, 5-(benzyloxy)-4-methoxy-2-nitrotoluene should be handled with care, as nitro compounds can be sensitive to heat and shock. The compound may have applications in the synthesis of pharmaceuticals or other organic compounds due to its unique structure and reactivity.

2495-83-2

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2495-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2495-83-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,9 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2495-83:
(6*2)+(5*4)+(4*9)+(3*5)+(2*8)+(1*3)=102
102 % 10 = 2
So 2495-83-2 is a valid CAS Registry Number.

2495-83-2Relevant academic research and scientific papers

Isomeric Monomethyl Ether Derivatives of (RS)-9,10-Dihydroxyaporphine ("Isoapomorphine") as Possible Products of Metabolism by Catechol-O-methyltransferase

Cannon, Joseph G.,Qijie, Pang

, p. 1079 - 1082 (1991)

The isomeric monomethyl ether derivatives of (RS)-9,10-dihydroxyaporphine ("isoapomorphine") were synthesized unequivocally as possible metabolites in catechol-O-methyltransferase (COMT) mediated O-methylation reactions.In vitro incubation studies revealed that isoapomorphine is not a substrate for the COMT using experimental conditions under which apomorphine (10,11-dihydroxyaporphine) is converted in high yield into its 10-methyl ether, apocodeine.The in vivo dopaminergic inactivity of isoapomorphine (as compared with that of apomorphine) seems to be due to factors other than metabolic inactivation by COMT.

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