2,2-Dimethylthiazolidine

Base Information

• Chemical Name: 2,2-Dimethylthiazolidine
• CAS No.: 19351-18-9
• Molecular Formula: C5H11NS
• Molecular Weight: 117.215
• Hs Code.: 2934999090
• European Community (EC) Number: 242-980-4
• DSSTox Substance ID: DTXSID3051832
• Nikkaji Number: J24.632H
• Wikidata: Q72472191
• Mol file: 19351-18-9.mol

Synonyms:2,2-dimethylthiazolidine;2,2-dimethylthiazolidine hydrochloride;DMTD

Chemical Property of 2,2-Dimethylthiazolidine

Chemical Property:

• Appearance/Colour: Colorless liquid
• Vapor Pressure: 1.5mmHg at 25°C
• Refractive Index: 1.5100-1.5140
• Boiling Point: 170 °C at 760 mmHg
• PKA: 8.97±0.40(Predicted)
• Flash Point: 56.6 °C
• PSA: 37.33000
• Density: 0.955 g/cm³
• LogP: 1.38770
• Storage Temp.: 2-8°C(protect from light)
• XLogP3: 0.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 117.06122053
• Heavy Atom Count: 7
• Complexity: 70.5

Purity/Quality:

99% ^*data from raw suppliers

2,2-Dimethyltetrahydrothiazole ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 10-36/37/38-25
• Safety Statements: 16-26-36/37/39-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(NCCS1)C
• Uses: 2,2-Dimethylthiazolidine is a promising radioprotectants.

Technology Process of 2,2-Dimethylthiazolidine

There total 4 articles about 2,2-Dimethylthiazolidine 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:

2-mercaptoethylamine hydrochloride (156-57-0) + acetone (67-64-1) → 2,2-dimethyl-1,3-thiazolidine (19351-18-9)

Guidance literature:

With methanol;

Reference yield:

ethyleneimine (151-56-4,9002-98-6) + acetone (67-64-1) → 2,2-dimethyl-1,3-thiazolidine (19351-18-9)

Guidance literature:

With hydrogen sulfide;

Reference yield:

ethyleneimine (151-56-4,9002-98-6) + hydrogen sulfide (7783-06-4) + acetone (67-64-1) → 2,2-dimethyl-1,3-thiazolidine (19351-18-9)

Guidance literature:

upstream raw materials:

ethyleneimine

acetone

2-mercaptoethylamine hydrochloride

hydrogen sulfide

Downstream raw materials:

1-phenyl-3-thiazolidin-3-yl-propan-1-one

C₂₅H₂₆FN₃O₃S₂

C₂₄H₂₄FN₃O₃S₂

C₂₀H₁₇FN₂O₂S₂