Naphtho[2,1-d]thiazole-2(3H)-thione

Base Information

Chemical Name:Naphtho[2,1-d]thiazole-2(3H)-thione
CAS No.:17931-26-9
Molecular Formula:C₁₁H₇NS₂
Molecular Weight:217.315
Hs Code.:2934999090
DSSTox Substance ID:DTXSID50498776
Wikidata:Q82349051
Mol file:17931-26-9.mol

Synonyms:Naphtho[2,1-d]thiazole-2(3H)-thione;17931-26-9;3H-benzo[g][1,3]benzothiazole-2-thione;Naphtho[2,1-d]thiazole-2(3H)-thione (9CI);Naphtho[2,1-d][1,3]thiazole-2(3H)-thione;SCHEMBL7119422;DTXSID50498776

Suppliers and Price of Naphtho[2,1-d]thiazole-2(3H)-thione

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

Alichem
Naphtho[2,1-d]thiazole-2(3H)-thione
25g
$ 2653.20

Alichem
Naphtho[2,1-d]thiazole-2(3H)-thione
10g
$ 1608.00

Alichem
Naphtho[2,1-d]thiazole-2(3H)-thione
5g
$ 1314.54

Total 3 raw suppliers

Chemical Property of Naphtho[2,1-d]thiazole-2(3H)-thione

Chemical Property:

PSA：79.93000
LogP:3.73820
XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:217.00199157
Heavy Atom Count:14
Complexity:254

Purity/Quality:

99% ^*data from raw suppliers

Naphtho[2,1-d]thiazole-2(3H)-thione ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC3=C2SC(=S)N3

Technology Process of Naphtho[2,1-d]thiazole-2(3H)-thione

There total 12 articles about Naphtho[2,1-d]thiazole-2(3H)-thione 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: 66.0%

: 90016-93-6
2-Amino-1-iodonaphthalene

: 67-68-5,8070-53-9
dimethyl sulfoxide

: 17931-26-9
naphtho[2,1-d]thiazole-2(3H)-thione

Guidance literature:: With potassium sulfide; at 140 ℃; for 12h; Sealed tube; Schlenk technique; Inert atmosphere;
DOI:10.1039/c8gc00477c

Reference yield: 45.0%

: 67-68-5,8070-53-9
dimethyl sulfoxide

: 91-59-8
naphthalen-2-ylamine

: 17931-26-9
naphtho[2,1-d]thiazole-2(3H)-thione

Guidance literature:: With copper(l) iodide; potassium sulfide; sulfur; at 140 ℃; for 36h; Schlenk technique; Inert atmosphere;

Reference yield:

: 2476-69-9
2-Amino-1-thiocyanatonaphthalene

: 17931-26-9
2-mercaptonaphtho<2,1-d>thiazole

Guidance literature:: Multi-step reaction with 2 steps

1: Na₂S / H₂O / 1 h / Heating

2: ethanol / 18 h / Heating

With sodium sulfide; In ethanol; water;