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Diethyl 2,2'-thiodiacetate

Base Information Edit
  • Chemical Name:Diethyl 2,2'-thiodiacetate
  • CAS No.:925-47-3
  • Molecular Formula:C8H14O4S
  • Molecular Weight:206.263
  • Hs Code.:29420000
  • European Community (EC) Number:213-117-9
  • NSC Number:12576
  • UNII:38N3YM4LAK
  • DSSTox Substance ID:DTXSID50239020
  • Nikkaji Number:J298.486E
  • Wikidata:Q72462231
  • Mol file:925-47-3.mol
Diethyl 2,2'-thiodiacetate

Synonyms:Diethyl 2,2'-thiodiacetate;925-47-3;Diethyl thioglycolate;ethyl 2-(2-ethoxy-2-oxoethyl)sulfanylacetate;DIETHYL 2,2-THIODIACETATE;38N3YM4LAK;Acetic acid, 2,2'-thiobis-, diethyl ester;EINECS 213-117-9;NSC-12576;diethyl 2,2'-sulfanediyldiacetate;Ethoxycarbonylmethylsulfanyl-acetic acid ethyl ester;3-Thiaglutaric acid diethyl ester;NSC12576;diethyl thiodiacetate;UNII-38N3YM4LAK;Diethyl thioglycolate, 96%;SCHEMBL8544332;thiodiacetic acid, diethyl ester;DTXSID50239020;MFCD00087932;NSC 12576;STL301892;2,2'-Thiodiacetic Acid Diethyl Ester;AKOS008952049;CS-W015317;2,2'-Thiobis(acetic acid ethyl) ester;2,2'-Thiodiglycolic Acid Diethyl Ester;AS-37625;D4147;FT-0630147;Acetic acid, 2,2'-thiobis-, 1,1'-diethyl ester;W-109616

Suppliers and Price of Diethyl 2,2'-thiodiacetate
Supply Marketing:Edit
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
  • Diethyl2,?2''-?Thiodiacetate
  • 5g
  • $ 85.00
  • TCI Chemical
  • Diethyl 2,2'-Thiodiglycolate >97.0%(GC)
  • 5g
  • $ 34.00
  • SynQuest Laboratories
  • Diethyl thioglycolate 98%
  • 1 g
  • $ 25.00
  • SynQuest Laboratories
  • Diethyl thioglycolate 98%
  • 5 g
  • $ 55.00
  • Frontier Specialty Chemicals
  • Diethylthioglycolate 99%
  • 5g
  • $ 141.00
  • Crysdot
  • Diethyl2,2'-thiodiacetate 97%
  • 100g
  • $ 399.00
  • Biosynth Carbosynth
  • Diethyl 2,2'-Thiodiglycolate
  • 5 g
  • $ 60.00
  • Biosynth Carbosynth
  • Diethyl 2,2'-Thiodiglycolate
  • 50 g
  • $ 347.00
  • Biosynth Carbosynth
  • Diethyl 2,2'-Thiodiglycolate
  • 25 g
  • $ 204.00
  • Biosynth Carbosynth
  • Diethyl 2,2'-Thiodiglycolate
  • 10 g
  • $ 102.00
Total 85 raw suppliers
Chemical Property of Diethyl 2,2'-thiodiacetate Edit
Chemical Property:
  • Vapor Pressure:0.0115mmHg at 25°C 
  • Melting Point:69-72 °C(lit.) 
  • Refractive Index:n20/D 1.467(lit.)  
  • Boiling Point:261.5 °C at 760 mmHg 
  • Flash Point:111.8°C 
  • PSA:77.90000 
  • Density:1.136 g/cm3 
  • LogP:0.84580 
  • Storage Temp.:Sealed in dry,Room Temperature 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:8
  • Exact Mass:206.06128010
  • Heavy Atom Count:13
  • Complexity:152
Purity/Quality:

99% *data from raw suppliers

Diethyl2,?2''-?Thiodiacetate *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CCOC(=O)CSCC(=O)OCC
  • Uses Diethyl 2,?2''-?Thiodiacetate is used in the synthesis of potent anticonvulsant agents. As well, used in the preparation of thienophenanthrene derivatives as polymer light-emitting devices and solar ccells.
Technology Process of Diethyl 2,2'-thiodiacetate

There total 16 articles about Diethyl 2,2'-thiodiacetate 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 sulfuric acid; Heating / reflux;
Guidance literature:
With sodium sulfide; In ethanol; at 50 ℃; for 1h; Inert atmosphere;
Guidance literature:
With sodium sulfide; In ethanol;
DOI:10.1021/jo01266a019
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