2-Ethylthiazolidine

Base Information

Chemical Name:2-Ethylthiazolidine
CAS No.:24050-09-7
Molecular Formula:C5H11 N S
Molecular Weight:117.215
Hs Code.:
DSSTox Substance ID:DTXSID20946895
Nikkaji Number:J48.806B
Mol file:24050-09-7.mol

Synonyms:2-Ethylthiazolidine;Thiazolidine, 2-ethyl-;24050-09-7;2-Ethyl-1,3-thiazolidine;BRN 0102763;starbld0044177;2-Ethyl-1,3-thiazolidine #;SCHEMBL4242727;DTXSID20946895;AKOS011421115;LS-151361

Suppliers and Price of 2-Ethylthiazolidine

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

Total 5 raw suppliers

Chemical Property of 2-Ethylthiazolidine

Chemical Property:

Vapor Pressure:0.602mmHg at 25°C
Boiling Point:188.3°Cat760mmHg
Flash Point:67.7°C
Density:0.962g/cm³
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:117.06122053
Heavy Atom Count:7
Complexity:56

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1NCCS1

Technology Process of 2-Ethylthiazolidine

There total 2 articles about 2-Ethylthiazolidine 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:

: 52-90-4
L-Cysteine

: 123-38-6
propionaldehyde

: 24050-09-7
2-ethylthiazolidine

: 554-14-3
2-Methylthiophene

: 2396-42-1
2,4,6-Triethyl-[1,3,5]trioxane

: 14250-96-5,16958-22-8,623-36-9
2-methyl-2-pentenal

: 124-07-2
Octanoic acid

: 100590-83-8
2-ethylthiazolidino<3,4-b>thiazolidine

Guidance literature:: In water; at 110 ℃; for 3h; Product distribution; addition of triglyceride, variation of solvent conditions;

Reference yield:

: 123-38-6
propionaldehyde

: 60-23-1
Cysteamine

: 24050-09-7
2-ethylthiazolidine

: 16982-46-0
2-ethyl-2-thiazoline

Guidance literature:: With phosphate buffer; In water; at 25 ℃; for 0.5h;
DOI:10.1021/jf9705633

Reference yield:

: 24050-09-7
2-ethylthiazolidine

: (+)-1-(4-(6-(2-ethylthiazolidine-3-carbonyl)benzo[d]thiazol-2-yl)-3-fluorobenzyl)azetidine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 1 h / 20 °C

2.1: hydrogenchloride; water / tetrahydrofuran / 4 h / 55 °C

3.1: acetic acid; N-ethyl-N,N-diisopropylamine / methanol; dichloromethane / 2 h / 20 °C

3.2: 1 h

4.1: chiralcel OJ-H / Resolution of racemate

5.1: water; lithium hydroxide / tetrahydrofuran

5.2: pH 6 / aq. phosphate buffer

With hydrogenchloride; water; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.10.069