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10,11-Dihydro-2-[(4-methyl-1-piperazinyl)methyl]-5H-dibenz[b,f]azepine is a complex organic compound belonging to the class of dibenzazepine derivatives. It is characterized by a dibenzazepine core structure, which is a type of tricyclic aromatic compound. The molecule features a 10,11-dihydro substitution, indicating the presence of two hydrogen atoms at positions 10 and 11, which are typically part of the dibenzazepine ring system. A 4-methyl-1-piperazinyl group is attached to the molecule, providing a methylated piperazine moiety that contributes to the compound's pharmacological properties. This specific chemical structure is known for its potential applications in the field of pharmaceuticals, particularly as a precursor or intermediate in the synthesis of drugs that target the central nervous system. The compound's exact role and mechanism of action would depend on the specific context in which it is used, but its structure suggests it may have activity related to its interaction with certain receptors or enzymes in the body.

64097-57-0

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64097-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64097-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,9 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64097-57:
(7*6)+(6*4)+(5*0)+(4*9)+(3*7)+(2*5)+(1*7)=140
140 % 10 = 0
So 64097-57-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H25N3/c1-22-10-12-23(13-11-22)15-16-6-9-20-18(14-16)8-7-17-4-2-3-5-19(17)21-20/h2-6,9,14,21H,7-8,10-13,15H2,1H3

64097-57-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(4-methylpiperazin-1-yl)methyl]-6,11-dihydro-5H-benzo[b][1]benzazepine

1.2 Other means of identification

Product number -
Other names N-methylpiperazinomethyl-2 dihydro-10,11 5H dibenzo<b,f>azepine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:64097-57-0 SDS

64097-57-0Downstream Products

64097-57-0Relevant academic research and scientific papers

TRICYCLIC COMPOUNDS

-

, (2008/06/13)

A tricyclic compound represented by the following formula (I): STR1 wherein R 1 represents hydrogen, halogen or lower alkyl; A represents cyano, carboxyl, tetrazolyl, cyano-substituted phenyl, carboxyl-substituted phenyl or tetrazolyl-substituted phenyl; V represents--(CH 2) m--wherein m is an integer of 0 to 2; W represents STR2 and Q 1--Q. sup.2--Q 3--Q 4 represents N=CH--CH=CH, CH=CH--CH= CH or CH 2--CH 2--CH. sub. 2--CH 2, STR3 and Q represents N or CH; X 1--X 2--X. sup.3 represents CH=CH--CH=CH, S--CH=CH or CH=CH--S; Y represents CH 2 CH 2 ; and Z. sup.1--Z 2 represents N--(CH. sub.2) n--wherein n is an integer of 1 to 3 or a pharmaceutically acceptable salt thereof.

Aminomethylation de l'homoacridane, de l'iminodibenzyle et de l'iminostilbene

Lehuede, Jacques,Vierfond, Jean-Michel,Miocque, Marcel

, p. 185 - 191 (2007/10/02)

The aminomethylation of 6,11-dihydro-5H-dibenzoazepine (HA), 10,11-dihydro-5H-dibenzoazepine (IDB) and dibenzoazepine (ISB) was studied in order to evaluate modifications of antidepressive activities of these tricyclic structures.By reaction with formalin and a secondary amine in ethanol medium acidified by means of acetic acid, homoacridane (HA) leads to a monosubstitution product on carbone 2 (yield 50percent).Iminodibenzyl (IDB) and iminostilbene (ISB) also give monoaminomethylation products in analogous position (yields are respectively 74 and 59percent).In each case, the optimum amount of acetic acid has been determined.If acetic acid is used as the solvent, diaminomethylation is observed in positions 2 and 8 (yiels are 74percent for IDB and 59percent for ISB).Structures of the isolated products have been studied by IR and 1H nmr.The postulated mechanism of aromatic electrophilic substitution is discussed with respect to various factors: differences in basicities of heterocyclic amines; electronic structures and nitrogen activation of aromatic tricyclic systems; influence of amount of acetic acid on salification equilibria.

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