Eudistomin N

Base Information

Chemical Name:Eudistomin N
CAS No.:59444-69-8
Molecular Formula:C11H7 Br N2
Molecular Weight:247.094
Hs Code.:
DSSTox Substance ID:DTXSID00974853
Nikkaji Number:J128.344H
Wikidata:Q27154927
Metabolomics Workbench ID:168454
ChEMBL ID:CHEMBL81169
Mol file:59444-69-8.mol

Synonyms:eudistomin N

Suppliers and Price of Eudistomin N

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
6-bromo-9H-Pyrido[3,4-b]indole 97.00%
25G
$ 5120.00

AccelPharmtech
6-bromo-9H-Pyrido[3,4-b]indole 97.00%
5G
$ 3300.00

AccelPharmtech
6-bromo-9H-Pyrido[3,4-b]indole 97.00%
1G
$ 1950.00

Total 3 raw suppliers

Chemical Property of Eudistomin N

Chemical Property:

Vapor Pressure:1.2E-07mmHg at 25°C
Boiling Point:443.6°C at 760 mmHg
Flash Point:222.1°C
PSA：28.68000
Density:1.699g/cm³
LogP:3.47860
XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:245.97926
Heavy Atom Count:14
Complexity:221

Purity/Quality:

99% ^*data from raw suppliers

6-bromo-9H-Pyrido[3,4-b]indole 97.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C=C1Br)C3=C(N2)C=NC=C3

Technology Process of Eudistomin N

There total 12 articles about Eudistomin N 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: 89.0%

: 244-63-3
betacarboline

: 59444-69-8
6-Brom-9H-pyrido<3,4-b>indol

Guidance literature:: With N-Bromosuccinimide; acetic acid; at 20 ℃; for 5h;
DOI:10.1039/c5ra16221a

Reference yield: 33.0%

: 244-63-3
betacarboline

: 144434-77-5
8-bromo-β-carboline

: 3,6-dibromonorharman hydrochloride

: 6,8-dibromonorharman hydrochloride

: 59444-69-8
6-Brom-9H-pyrido<3,4-b>indol

Guidance literature:: With N-Bromosuccinimide; silica gel; In dichloromethane; at 18 ℃; for 24h;
DOI:10.1016/S0040-4020(01)90362-X

Reference yield: 25.0%

: 244-63-3
betacarboline

: 144434-77-5
8-bromo-β-carboline

: 144434-80-0
3,6,8-tribromonor-harmane

: 6,8-dibromonorharman hydrochloride

: 59444-69-8
6-Brom-9H-pyrido<3,4-b>indol

Guidance literature:: With N-Bromosuccinimide; silica gel; In dichloromethane; at 18 ℃; for 36h; Further byproducts given;
DOI:10.1016/S0040-4020(01)90362-X