2-Aminothiazol-4(5H)-one hydrochloride

Base Information

• Chemical Name: 2-Aminothiazol-4(5H)-one hydrochloride
• CAS No.: 2192-06-5
• Molecular Formula: C3H4 N2 O S . Cl H
• Molecular Weight: 152.605
• Hs Code.: 2934100090
• European Community (EC) Number: 606-864-0
• NSC Number: 55654
• DSSTox Substance ID: DTXSID80382038
• Mol file: 2192-06-5.mol

Synonyms:2192-06-5;2-Aminothiazol-4(5H)-one hydrochloride;2-Aminothiazolinone hydrochloride;2-Amino-4,5-dihydro-1,3-thiazol-4-one hydrochloride;2-Aminothiazolinone HCl;2-amino-1,3-thiazol-4-one;hydrochloride;2-Amino-4,5-dihydro-1,3-thiazol-4-one, HCl;2-Aminothiazole-4-one hydrochloride;MFCD00277945;2-Amino-1,3-thiazol-4(5H)-one hydrochloride;C3H5ClN2OS;SCHEMBL5520106;Pseudothiohydantoin hydrochloride;2-Amino-4,5-dihydro-4-oxo-1,3-thiazole hydrochloride;DTXSID80382038;4-Thiazolidinone, monohydrochloride;NSC55654;2-aminothiazolin-4-one hydrochloride;4(5H)-Thiazolone, monohydrochloride;MFCD00463374;NSC 55654;NSC-55654;AKOS025142171;2-Aminothiazol-4(5H)-onehydrochloride;2-Imino-4-thiazolidinone hydrochloride;PS-8912;2-iminothiazolidine-4-one hydrochloride salt;2-Imino-4-oxo-1,3-thiazolidine hydrochloride;EN300-306150;A911598;W-204263;2-Amino-1,3-thiazol-4(5H)-one--hydrogen chloride (1/1)

Chemical Property of 2-Aminothiazol-4(5H)-one hydrochloride

Chemical Property:

• Vapor Pressure: 0.0182mmHg at 25°C
• Melting Point: >350 °C
• Boiling Point: 253.5°Cat760mmHg
• Flash Point: 107.1°C
• PSA: 80.75000
• Density: g/cm³
• LogP: 0.51240
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 151.9811117
• Heavy Atom Count: 8
• Complexity: 131

Purity/Quality:

98%min ^*data from raw suppliers

2-Amino-4,5-dihydro-1,3-thiazol-4-onehydrochloride ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 43
• Safety Statements: 36/37

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(=O)N=C(S1)N.Cl

Technology Process of 2-Aminothiazol-4(5H)-one hydrochloride

There total 1 articles about 2-Aminothiazol-4(5H)-one hydrochloride 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: 75.0%

carboxymethylisothiourea hydrochloride (5425-78-5) → 2-Amino-4-thiazolinone hydrochloride (2192-06-5)

Guidance literature:

In acetone; Heating;

Reference yield:

water (7732-18-5) + 2-Amino-4-thiazolinone hydrochloride (2192-06-5) → thiazoline-2,4-dione (2295-31-0) + ammonia (7664-41-7)

Guidance literature:

Reference yield:

phosphorus (III) oxychloride (21295-50-1) + 2-Amino-4-thiazolinone hydrochloride (2192-06-5) → 2-amino-4-chloro-5-formyl-1,3-thiazole (76874-79-8)

Guidance literature:

With sodium acetate; In water; N,N-dimethyl-formamide;

upstream raw materials:

carboxymethylisothiourea hydrochloride

Downstream raw materials:

thiazoline-2,4-dione

ammonia

2-amino-4-chloro-5-formyl-1,3-thiazole

Refernces