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Saccharin N-(2-acetic acid ethyl ester)

Base Information
  • Chemical Name:Saccharin N-(2-acetic acid ethyl ester)
  • CAS No.:24683-20-3
  • Molecular Formula:C11H11 N O5 S
  • Molecular Weight:269.278
  • Hs Code.:2934999090
  • European Community (EC) Number:607-416-7
  • UNII:KN712V27AV
  • DSSTox Substance ID:DTXSID50179412
  • Wikidata:Q27282339
  • Pharos Ligand ID:TMQCL8GZ3Y2T
  • ChEMBL ID:CHEMBL3125563
  • Mol file:24683-20-3.mol
Saccharin N-(2-acetic acid ethyl ester)

Synonyms:24683-20-3;Saccharin N-(2-acetic acid ethyl ester);Ethyl (1,1-dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)acetate;ethyl 2-(1,1,3-trioxo-1,2-benzothiazol-2-yl)acetate;Saccharin N-(2-Acetic Acid Ethyl Ester)(Piroxicam Impurity E);Piroxicam impurity E [EP];UNII-KN712V27AV;KN712V27AV;CHEMBL3125563;ethyl (1,1-dioxido-3-oxo-1,2-benzothiazol-2(3H)-yl)acetate;Ethyl2,3-dihydro-3-oxo-1,2-benzisothiazole-2-acetate-1,1-dioxide;1,2-Benzisothiazole-2(3H)-acetic acid, 3-oxo-, ethyl ester, 1,1-dioxide;EC 607-416-7;ethyl 2-(1,1,3-trioxo-2,3-dihydro-1lambda6,2-benzothiazol-2-yl)acetate;Ethyl 2-(1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)acetate;(Piroxicam Impurity E)";ChemDiv1_000366;Oprea1_631494;Oprea1_858121;SCHEMBL14884779;HMS588A14;DTXSID50179412;HMS3429B03;BDBM50496460;MFCD00688886;STK136579;AKOS000418951;CCG-113731;(1,1,3-Trioxo-1,3-dihydro-1lambda*6*-benzo[d]isothiazol-2-yl)-acetic acid ethyl;PIROXICAM IMPURITY E [EP IMPURITY];CS-0127725;FT-0674495;EN300-299011;SR-01000398864;SR-01000398864-1;Q27282339;Z51115233;Ethyl 3-oxo-1,2-benzoisothiazoline-2-acetate 1,1-dioxide;Ethyl2-(1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)acetate;Benzo[d]isothiazol-3-one, 2-(2-ethoxy-2-oxoethyl)-, 1,1-dioxide;Ethyl (1,1-dioxido-3-oxo-1,2-benzisothiazol-2(3H)-yl)acetate #;ethyl 2-(1,1,3-trioxo-2,3-dihydro-1|E?,2-benzothiazol-2-yl)acetate

Suppliers and Price of Saccharin N-(2-acetic acid 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
  • Packaging
  • price
  • TRC
  • SaccharinN-(2-AceticAcidEthylEster)(PiroxicamImpurityE)
  • 250mg
  • $ 765.00
  • TRC
  • SaccharinN-(2-AceticAcidEthylEster)(PiroxicamImpurityE)
  • 25mg
  • $ 115.00
  • Biosynth Carbosynth
  • 3-Oxo-1,2-benzisothiazole-2(3H)-acetic acid ethyl ester 1,1-dioxide
  • 250 mg
  • $ 150.00
  • Biosynth Carbosynth
  • 3-Oxo-1,2-benzisothiazole-2(3H)-acetic acid ethyl ester 1,1-dioxide
  • 100 mg
  • $ 100.00
  • Biosynth Carbosynth
  • 3-Oxo-1,2-benzisothiazole-2(3H)-acetic acid ethyl ester 1,1-dioxide
  • 50 mg
  • $ 57.50
  • American Custom Chemicals Corporation
  • PIROXICAM EP IMPURITY E 95.00%
  • 5MG
  • $ 456.49
Total 13 raw suppliers
Chemical Property of Saccharin N-(2-acetic acid ethyl ester)
Chemical Property:
  • Vapor Pressure:5.45E-08mmHg at 25°C 
  • Melting Point:106℃ 
  • Refractive Index:1.584 
  • Boiling Point:441.4°C at 760 mmHg 
  • PKA:-16.17±0.20(Predicted) 
  • Flash Point:220.8°C 
  • PSA:89.13000 
  • Density:1.442g/cm3 
  • LogP:1.41290 
  • Storage Temp.:-20°C Freezer, Under inert atmosphere 
  • Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly) 
  • XLogP3:0.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:4
  • Exact Mass:269.03579362
  • Heavy Atom Count:18
  • Complexity:453
Purity/Quality:

99.9% *data from raw suppliers

SaccharinN-(2-AceticAcidEthylEster)(PiroxicamImpurityE) *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)CN1C(=O)C2=CC=CC=C2S1(=O)=O
  • Uses Piroxicam impurity E.
Technology Process of Saccharin N-(2-acetic acid ethyl ester)

There total 11 articles about Saccharin N-(2-acetic acid 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:
Guidance literature:
With 3,3-dimethyldioxirane; In acetone; at 25 ℃; Cooling;
DOI:10.1016/j.bmcl.2009.12.001
Guidance literature:
With potassium fluoride; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate; at 85 ℃; for 1.5h;
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