2-Thiazoline, 2-(1-naphthylamino)-

Base Information

• Chemical Name: 2-Thiazoline, 2-(1-naphthylamino)-
• CAS No.: 35160-17-9
• Molecular Formula: C13H12N2S
• Molecular Weight: 228.3128
• NSC Number: 135968
• UNII: LLI7E0MLR7
• DSSTox Substance ID: DTXSID20188657
• Nikkaji Number: J1.858.286D
• Wikidata: Q83060477
• ChEMBL ID: CHEMBL1565537
• Mol file: 35160-17-9.mol

Synonyms:2-Thiazoline, 2-(1-naphthylamino)-;2-(1-Naphthylamino)-2-thiazoline;LLI7E0MLR7;35160-17-9;NSC-135968;N-(naphthalen-1-yl)-4,5-dihydro-1,3-thiazol-2-amine;NSC 135968;BRN 0163062;2-Thiazolamine, 4,5-dihydro-N-1-naphthalenyl-;NSC135968;UNII-LLI7E0MLR7;4-27-00-04558 (Beilstein Handbook Reference);MLS000066174;CHEMBL1565537;DTXSID20188657;OPHJVMLHMZPRDG-UHFFFAOYSA-N;HMS1595I17;HMS2307K14;STK377802;AKOS003320209;SDCCGMLS-0037382.P002;SMR000079768;N-1-naphthyl-4,5-dihydro-1,3-thiazol-2-amine;SR-01000289219;2-Thiazolamine, 4,5-dihydro-N-(1-naphthalenyl)-;SR-01000289219-1;4,5-DIHYDRO-N-1-NAPHTHALENYL-2-THIAZOLAMINE

Chemical Property of 2-Thiazoline, 2-(1-naphthylamino)-

Chemical Property:

• Vapor Pressure: 9.08E-07mmHg at 25°C
• Boiling Point: 405°Cat760mmHg
• Flash Point: 198.7°C
• Density: 1.26g/cm³
• XLogP3: 3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 228.07211956
• Heavy Atom Count: 16
• Complexity: 277

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CSC(=N1)NC2=CC=CC3=CC=CC=C32

Technology Process of 2-Thiazoline, 2-(1-naphthylamino)-

There total 5 articles about 2-Thiazoline, 2-(1-naphthylamino)- 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: 64.0%

sulfuric acid mono-(2-amino-ethyl ester) (926-39-6) + 1-isothiocyanatonaphthalene (551-06-4) → 2-α-Naphthylamino-Δ2-thiazolin (35160-17-9)

Guidance literature:

With sodium hydroxide; ethanol;

Reference yield:

1-(2-hydroxy-ethyl)-3-naphthalen-1-yl-thiourea (52266-64-5) → 2-α-Naphthylamino-Δ2-thiazolin (35160-17-9)

Guidance literature:

With hydrogenchloride; at 100 - 105 ℃; for 6h;

Reference yield:

aziridine-1-carbothioic acid-[1]naphthylamide (108874-53-9) → 2-α-Naphthylamino-Δ2-thiazolin (35160-17-9)

Guidance literature:

With hydrogenchloride;

DOI:10.1002/ardp.19582910906

upstream raw materials:

aziridine-1-carbothioic acid-[1]naphthylamide

1-(2-hydroxy-ethyl)-3-naphthalen-1-yl-thiourea

sulfuric acid mono-(2-amino-ethyl ester)

1-isothiocyanatonaphthalene

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