1,3,4-Thiadiazol-2-amine, N-(4-iodophenyl)-5-(2-(10H-phenothiazin-10-yl)ethyl)-

Base Information

Chemical Name:1,3,4-Thiadiazol-2-amine, N-(4-iodophenyl)-5-(2-(10H-phenothiazin-10-yl)ethyl)-
CAS No.:180793-94-6
Molecular Formula:C22H17IN4S2
Molecular Weight:528.4316
Hs Code.:
DSSTox Substance ID:DTXSID30171015
Nikkaji Number:J827.039B
Wikidata:Q83041052
Mol file:180793-94-6.mol

Synonyms:180793-94-6;1,3,4-Thiadiazol-2-amine, N-(4-iodophenyl)-5-(2-(10H-phenothiazin-10-yl)ethyl)-;N-(4-Iodophenyl)-5-(2-(10H-phenothiazin-10-yl)ethyl)-1,3,4-thiadiazol-2-amine;2-((N-Phenothiazinyle)ethylene)-5-(iodophenyleamino)-1,3,4-thiadiazole [French];2-((N-Phenothiazinyle)ethylene)-5-(iodophenyleamino)-1,3,4-thiadiazole;N-(4-IODOPHENYL)-5-[2-(10H-PHENOTHIAZIN-10-YL)ETHYL]-1,3,4-THIADIAZOL-2-AMINE;C22H17IN4S2;DTXSID30171015;C22-H17-I-N4-S2;LS-150226

Suppliers and Price of 1,3,4-Thiadiazol-2-amine, N-(4-iodophenyl)-5-(2-(10H-phenothiazin-10-yl)ethyl)-

Supply Marketing:

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

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Chemical Property of 1,3,4-Thiadiazol-2-amine, N-(4-iodophenyl)-5-(2-(10H-phenothiazin-10-yl)ethyl)-

Chemical Property:

Vapor Pressure:1.75E-16mmHg at 25°C
Boiling Point:644.1°Cat760mmHg
Flash Point:343.4°C
Density:1.656g/cm³
XLogP3:6.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:527.99394
Heavy Atom Count:29
Complexity:511

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)N(C3=CC=CC=C3S2)CCC4=NN=C(S4)NC5=CC=C(C=C5)I

Technology Process of 1,3,4-Thiadiazol-2-amine, N-(4-iodophenyl)-5-(2-(10H-phenothiazin-10-yl)ethyl)-

There total 6 articles about 1,3,4-Thiadiazol-2-amine, N-(4-iodophenyl)-5-(2-(10H-phenothiazin-10-yl)ethyl)- 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: 69.0%

: 180793-86-6
C₂₂H₁₉IN₄OS₂

: 180793-94-6
(4-Iodo-phenyl)-[5-(2-phenothiazin-10-yl-ethyl)-[1,3,4]thiadiazol-2-yl]-amine

Guidance literature:: With sulfuric acid; for 24h; Ambient temperature;
DOI:10.1080/10426509608029654

Reference yield:

: 92-84-2
10H-phenothiazine

: 180793-94-6
(4-Iodo-phenyl)-[5-(2-phenothiazin-10-yl-ethyl)-[1,3,4]thiadiazol-2-yl]-amine

Guidance literature:: Multi-step reaction with 6 steps

1: Triton B

2: NaOH / Heating

3: H⁺ / Heating

4: N₂H₄ / ethanol / Heating

5: 87 percent / ethanol / Heating

6: 69 percent / conc. H₂SO₄ / 24 h / Ambient temperature

With sodium hydroxide; sulfuric acid; hydrogen cation; N-benzyl-trimethylammonium hydroxide; hydrazine; In ethanol;
DOI:10.1080/10426509608029654

Reference yield:

: 1698-80-2
10H-phenothiazine-10-propanenitrile

: 180793-94-6
(4-Iodo-phenyl)-[5-(2-phenothiazin-10-yl-ethyl)-[1,3,4]thiadiazol-2-yl]-amine

Guidance literature:: Multi-step reaction with 5 steps

1: NaOH / Heating

2: H⁺ / Heating

3: N₂H₄ / ethanol / Heating

4: 87 percent / ethanol / Heating

5: 69 percent / conc. H₂SO₄ / 24 h / Ambient temperature

With sodium hydroxide; sulfuric acid; hydrogen cation; hydrazine; In ethanol;
DOI:10.1080/10426509608029654