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N-benzyl-3,4,5,6-tetrahydro-2H-azepin-7-amine is a chemical compound with the molecular formula C12H18N2. It is a derivative of azepine, a seven-membered heterocyclic ring containing one nitrogen atom. The compound features a benzyl group attached to the nitrogen atom, which is part of a tetrahydroazepine ring. This structure is significant in medicinal chemistry, as it can be found in various pharmaceuticals and bioactive molecules. The compound is known for its potential applications in the development of drugs targeting the central nervous system, due to its ability to interact with specific receptors or enzymes. Its synthesis and properties are of interest to researchers in the field of organic chemistry and drug discovery.

7048-72-8

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7048-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7048-72-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,4 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7048-72:
(6*7)+(5*0)+(4*4)+(3*8)+(2*7)+(1*2)=98
98 % 10 = 8
So 7048-72-8 is a valid CAS Registry Number.
InChI:InChI=1/C27H26Cl2N4O4/c1-17-20(16-30-33(17)19-5-3-2-4-6-19)25(34)23-24(18-7-8-21(28)22(29)15-18)32(27(36)26(23)35)10-9-31-11-13-37-14-12-31/h2-8,15-16,24,34H,9-14H2,1H3

7048-72-8Downstream Products

7048-72-8Relevant academic research and scientific papers

Lactamimides in the treatment of drug-resistant protozoal infections

-

, (2008/06/13)

Standard antiprotozoal agents in conjunction with a lactamimide derivative are effective pharmaceutical compositions for the treatment of drug-resistant protozoal infection, particularly, drug-resistant malarial infection in humans.

THE CHEMISTRY OF LACTIM ETHERS. V. REACTION OF LACTIM THIOETHERS WITH β-AMINOESTERS

Takahata, Hiroki,Tomoguchi, Akira,Yamazaki, Takao

, p. 2525 - 2530 (2007/10/02)

Reaction of a cyclic β-aminoester such as 2-ethoxycarbonylmethylpiperidine (5) with the lactim thioethers 1b and 1c gave a 10-membered cyclic diamide (7) and an 11-membered ring compound (9), respectively.On the other hand, though acyclic β-aminoesters (6) reacted with 1 to afford methyl 3-methylthiopropionate (11), N-alkyl 3-methylthiopropionamide (12), lactams (13), and amidines (14), no cyclic diamide was obtained.Keywords: - lactim thioethers; cyclic β-aminoesters; acyclic β-aminoesters; cyclic diamide; medium-ring; methyl 3-methylthiopropionate; N-alkyl 3-methylthiopionamide; amidines; lactams; β-lactmams

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