Damirone B

Base Information

Chemical Name:Damirone B
CAS No.:138683-67-7
Molecular Formula:C11H10N2O2
Molecular Weight:202.213
Hs Code.:
NSC Number:700004
DSSTox Substance ID:DTXSID40930190
Nikkaji Number:J825.292K
Wikidata:Q82905432
Metabolomics Workbench ID:136140
ChEMBL ID:CHEMBL462951
Mol file:138683-67-7.mol

Synonyms:Damirone B;138683-67-7;5-Methyl-4,5-dihydropyrrolo[4,3,2-de]quinoline-7,8(1H,3H)-dione;Pyrrolo[4,3,2-de]quinoline-7,8-dione, 1,3,4,5-tetrahydro-5-methyl- (9CI);7-methyl-2,7-diazatricyclo[6.3.1.04,12]dodeca-1(12),3,8-triene-10,11-dione;CHEMBL462951;SCHEMBL9263961;JYLGJUYDUWMFOL-UHFFFAOYSA-;DTXSID40930190;5-methyl-1,3,4,5-tetrahydropyrrolo[4,3,2-de]quinoline-7,8-dione;NSC700004;NSC 700004;NSC-700004;Pyrrolo(4,3,2-de)quinoline-7,8-dione, 1,3,4,5-tetrahydro-5-methyl-;Pyrrolo[4,2-de]quinoline-7,8-dione, 1,3,4,5-tetrahydro-5-methyl-;InChI=1/C11H10N2O2/c1-13-3-2-6-5-12-10-9(6)7(13)4-8(14)11(10)15/h4-5,12H,2-3H2,1H3

Suppliers and Price of Damirone B

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

AccelPharmtech
1,3,4,5-tetrahydro-5-methyl-Pyrrolo[4,3,2-de]quinoline-7,8-dione 97.00%
25G
$ 9900.00

AccelPharmtech
1,3,4,5-tetrahydro-5-methyl-Pyrrolo[4,3,2-de]quinoline-7,8-dione 97.00%
5G
$ 5270.00

Total 1 raw suppliers

Chemical Property of Damirone B

Chemical Property:

PSA：53.17000
LogP:0.54680
XLogP3:0.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:202.074227566
Heavy Atom Count:15
Complexity:375

Purity/Quality:: 1,3,4,5-tetrahydro-5-methyl-Pyrrolo[4,3,2-de]quinoline-7,8-dione 97.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN1CCC2=CNC3=C2C1=CC(=O)C3=O

Technology Process of Damirone B

There total 33 articles about Damirone B which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 76.0%

: 148613-96-1
1,3,4,5,7,8-hexahydro-5-methyl-1-(4-methylbenzenesulfonyl)pyrrolo<4,3,2-de>quinoline-7,8-dione

: 138683-67-7
Damirone B

Guidance literature:: With sodium hydroxide; In methanol; at 25 ℃; for 0.5h;
DOI:10.1016/S0040-4039(00)60427-6

Reference yield: 50.0%

: 160208-44-6
7-Methoxy-2,4-dihydropyrrolo<4,3,2-de>quinolin-8(1H)-one

: 74-88-4
methyl iodide

: 138683-67-7
Damirone B

Guidance literature:: 7-Methoxy-2,4-dihydropyrrolo<4,3,2-de>quinolin-8(1H)-one; methyl iodide; In acetone; at 60 ℃; for 0.5h; Sealed tube; Inert atmosphere;

With potassium iodide; In acetone; at 70 ℃; for 7h; Sealed tube; Inert atmosphere;
DOI:10.1016/j.tet.2012.09.034