Thiosulfuric acid, S-(2-imino-2-((2-(2-oxo-1-pyrrolidinyl)ethyl)amino)ethyl) ester

Base Information

Chemical Name:Thiosulfuric acid, S-(2-imino-2-((2-(2-oxo-1-pyrrolidinyl)ethyl)amino)ethyl) ester
CAS No.:117018-96-9
Molecular Formula:C₈H₁₅N₃O₄S₂
Molecular Weight:281.357
Hs Code.:
DSSTox Substance ID:DTXSID70151679

Synonyms:BRN 5589935;Thiosulfuric acid, S-(2-imino-2-((2-(2-oxo-1-pyrrolidinyl)ethyl)amino)ethyl) ester;N-(beta-(2-Pyrrolidon-1-yl)ethyl)-alpha-thiosulfoacetamidine;117018-96-9;DTXSID70151679;LS-153419

Suppliers and Price of Thiosulfuric acid, S-(2-imino-2-((2-(2-oxo-1-pyrrolidinyl)ethyl)amino)ethyl) ester

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
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price

Total 5 raw suppliers

Chemical Property of Thiosulfuric acid, S-(2-imino-2-((2-(2-oxo-1-pyrrolidinyl)ethyl)amino)ethyl) ester

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.61g/cm³
XLogP3:-1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:281.05039832
Heavy Atom Count:17
Complexity:402

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(=O)N(C1)CCN=C(CSS(=O)(=O)O)N

Technology Process of Thiosulfuric acid, S-(2-imino-2-((2-(2-oxo-1-pyrrolidinyl)ethyl)amino)ethyl) ester

There total 2 articles about Thiosulfuric acid, S-(2-imino-2-((2-(2-oxo-1-pyrrolidinyl)ethyl)amino)ethyl) ester 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: 70.7%

: N-<β-(2-Pyrrolidon-1-yl)ethyl>-α-chloroacetamidine hydrochloride

: 117018-96-9
N-<β-(2-Pyrrolidon-1-yl)ethyl>-α-thiosulfoacetamidine

Guidance literature:: With thallium(I) thiosulfate; In water; for 1h; Heating;
DOI:10.1007/BF00763382

Reference yield:

: 24935-08-8
1-(2-aminoethyl)-2-pyrrolidinone

: 117018-96-9
N-<β-(2-Pyrrolidon-1-yl)ethyl>-α-thiosulfoacetamidine

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) MeONa, 2.) HCl / 1.) MeOH, room temp., 2 h, 2.) MeOH, 6 h

2: 70.7 percent / thallium thiosulfate / H₂O / 1 h / Heating

With hydrogenchloride; thallium(I) thiosulfate; sodium methylate; In water;
DOI:10.1007/BF00763382