JWH 200 2'-naphthyl isomer

Base Information

Chemical Name:JWH 200 2'-naphthyl isomer
CAS No.:133438-66-1
Molecular Formula:C25H24N2O2
Molecular Weight:384.47000
Hs Code.:
DSSTox Substance ID:DTXSID401017325
ChEMBL ID:CHEMBL307073
Mol file:133438-66-1.mol

Synonyms:JWH 200 2'-naphthyl isomer;133438-66-1;JWH 200 2/'-naphthyl isomer;CHEMBL307073;[1-(2-morpholin-4-ylethyl)indol-3-yl]-naphthalen-2-ylmethanone;SCHEMBL21179005;ZESGOIBULDUMRS-UHFFFAOYSA-N;DTXSID401017325;BDBM50032622;[1-(2-Morpholin-4-yl-ethyl)-1H-indol-3-yl]-naphthalen-2-yl-methanone

Suppliers and Price of JWH 200 2'-naphthyl isomer

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

Cayman Chemical
JWH 200 2'-naphthyl isomer ≥98%
10mg
$ 392.00

Cayman Chemical
JWH 200 2'-naphthyl isomer ≥98%
5mg
$ 221.00

Cayman Chemical
JWH 200 2'-naphthyl isomer ≥98%
1mg
$ 49.00

AK Scientific
JWH2002'-naphthylisomer
10mg
$ 629.00

AK Scientific
JWH2002'-naphthylisomer
1mg
$ 166.00

Total 8 raw suppliers

Chemical Property of JWH 200 2'-naphthyl isomer

Chemical Property:

PSA：34.47000
LogP:4.29560
XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:384.183778013
Heavy Atom Count:29
Complexity:561

Purity/Quality:

99% ^*data from raw suppliers

JWH 200 2'-naphthyl isomer ≥98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COCCN1CCN2C=C(C3=CC=CC=C32)C(=O)C4=CC5=CC=CC=C5C=C4

Technology Process of JWH 200 2'-naphthyl isomer

There total 2 articles about JWH 200 2'-naphthyl isomer 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:

: 72395-48-3
1-<2-(4-morpholinyl)ethyl>-1H-indole

: 2243-83-6
2-naphthaloyl chloride

: 133438-66-1
[1-[2-(4-morpholinyl)ethyl]-1H-indol-3-yl]-2-naphthalenylmethanone

Guidance literature:: With ethylaluminum dichloride; In dichloromethane; toluene; at -78 - 20 ℃; Yield given;
DOI:10.1021/jm00016a013

Reference yield:

: 93-09-4
naphthalene-2-carboxylate

: 133438-66-1
[1-[2-(4-morpholinyl)ethyl]-1H-indol-3-yl]-2-naphthalenylmethanone

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂, DMF / Ambient temperature

2: EtAlCl₂ / CH₂Cl₂; toluene / -78 - 20 °C

With thionyl chloride; ethylaluminum dichloride; N,N-dimethyl-formamide; In dichloromethane; toluene;
DOI:10.1021/jm00016a013