N-Naphthyl-1,2,3,4-thiatriazol-5-amine

Base Information

Chemical Name:N-Naphthyl-1,2,3,4-thiatriazol-5-amine
CAS No.:10320-97-5
Molecular Formula:C11H8 N4 S
Molecular Weight:228.277
Hs Code.:2933990090
European Community (EC) Number:233-704-3
DSSTox Substance ID:DTXSID50145697
Nikkaji Number:J236.489A
Wikidata:Q83010274
Mol file:10320-97-5.mol

Synonyms:10320-97-5;N-Naphthyl-1,2,3,4-thiatriazol-5-amine;N-naphthalen-1-ylthiatriazol-5-amine;EINECS 233-704-3;5-(1-NAPHTHYL-AMINO)-1,2,3,4-THIA-TRIAZOLE;N-(1-Naphthyl)-1,2,3,4-thiatriazol-5-amine;SCHEMBL9405249;DTXSID50145697;AKOS024325558;5-(1-Naphthylamino)-1,2,3,4-thiatriazole;N-(1-Naphthyl)-1,2,3,4-thiatriazol-5-amine #;1,2,3,4-Thiatriazol-5-amine, N-1-naphthalenyl-

Suppliers and Price of N-Naphthyl-1,2,3,4-thiatriazol-5-amine

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

TRC
5-(1-Naphthyl-amino)-1,2,3,4-thia-triazole
50mg
$ 45.00

Total 8 raw suppliers

Chemical Property of N-Naphthyl-1,2,3,4-thiatriazol-5-amine

Chemical Property:

Vapor Pressure:7.84E-07mmHg at 25°C
Boiling Point:406.9°Cat760mmHg
Flash Point:199.9°C
PSA：82.17000
Density:1.438g/cm³
LogP:2.25180
XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:228.04696745
Heavy Atom Count:16
Complexity:238

Purity/Quality:

98%,99%, ^*data from raw suppliers

5-(1-Naphthyl-amino)-1,2,3,4-thia-triazole ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC=C2NC3=NN=NS3

Technology Process of N-Naphthyl-1,2,3,4-thiatriazol-5-amine

There total 4 articles about N-Naphthyl-1,2,3,4-thiatriazol-5-amine 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:

: 42135-78-4
4-(1-naphthyl)-3-thiosemicarbazide

: 10320-97-5
N-(naphthalen-1-yl)-1,2,3,4-thiatriazol-5-amine

Guidance literature:: With hydrogenchloride; sodium nitrate; In water; at 10 - 15 ℃; for 0.666667h;

Reference yield:

: 134-32-7
1-amino-naphthalene

: 10320-97-5
N-(naphthalen-1-yl)-1,2,3,4-thiatriazol-5-amine

Guidance literature:: Multi-step reaction with 3 steps

1: liq. NH₃ / -30 °C

2: hydrazine hydrate, sodium chloroacetate / aq. ethanol

3: sodium nitrate, hydrochloric acid / H₂O / 0.67 h / 10 - 15 °C

With hydrogenchloride; sodium nitrate; ammonia; sodium monochloroacetic acid; hydrazine hydrate; In ethanol; water;

Reference yield:

: 15866-95-2
naphthalen-1-yl-dithiocarbamic acid; ammonium salt

: 10320-97-5
N-(naphthalen-1-yl)-1,2,3,4-thiatriazol-5-amine

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine hydrate, sodium chloroacetate / aq. ethanol

2: sodium nitrate, hydrochloric acid / H₂O / 0.67 h / 10 - 15 °C

With hydrogenchloride; sodium nitrate; sodium monochloroacetic acid; hydrazine hydrate; In ethanol; water;