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Ethyl 1,3-dithiane-2-carboxylate

Base Information Edit
  • Chemical Name:Ethyl 1,3-dithiane-2-carboxylate
  • CAS No.:20462-00-4
  • Molecular Formula:C7H12 O2 S2
  • Molecular Weight:192.303
  • Hs Code.:29349990
  • European Community (EC) Number:243-838-4
  • UNII:DRA87T4JKT
  • DSSTox Substance ID:DTXSID50174427
  • Nikkaji Number:J208.387F
  • Wikidata:Q72474666
  • Mol file:20462-00-4.mol
Ethyl 1,3-dithiane-2-carboxylate

Synonyms:Ethyl 1,3-dithiane-2-carboxylate;20462-00-4;1,3-Dithiane-2-carboxylic acid ethyl ester;1,3-Dithiane-2-carboxylic acid, ethyl ester;Carboethoxy-1,3-dithiane;2-Carboethoxy-1,3-dithiane;C7H12O2S2;DRA87T4JKT;m-Dithiane-2-carboxylic acid, ethyl ester;EINECS 243-838-4;MFCD00006657;[1,3]dithiane-2-carboxylic acid ethyl ester;2-(Ethoxycarbonyl)-1,3-dithiane;Ethyl1,3-Dithiane-2-carboxylate;UNII-DRA87T4JKT;2-carboethoxy 1,3-dithiane;SCHEMBL113220;2-ethoxycarbonyl-1,3-dithiane;ethyl 1,3 dithiane carboxylate;ANEDZEVDORCLPM-UHFFFAOYSA-;DTXSID50174427;ethyl 1,3-dithian-2-carboxylate;2-(ethoxycarbonyl)-1,3-dithiane;C7-H12-O2-S2;AKOS015856659;2-(2-phenyliminothiazolidin-3-yl)ethanol;BS-43937;SY047739;CS-0020890;D1648;FT-0606728;D89899;A814584;J-013340;Ethyl 1,3-dithiane-2-carboxylate, technical, >=90% (GC)

Suppliers and Price of Ethyl 1,3-dithiane-2-carboxylate
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
  • Ethyl 1,3-dithiane-2-carboxylate
  • 100mg
  • $ 60.00
  • TRC
  • Ethyl 1,3-dithiane-2-carboxylate
  • 50mg
  • $ 45.00
  • TCI Chemical
  • Ethyl 1,3-Dithiane-2-carboxylate >98.0%(GC)
  • 1g
  • $ 31.00
  • TCI Chemical
  • Ethyl 1,3-Dithiane-2-carboxylate >98.0%(GC)
  • 5g
  • $ 87.00
  • Synthonix
  • 1,3-Dithiane-2-carboxylicacidethylester 97%
  • 5g
  • $ 70.00
  • Synthonix
  • 1,3-Dithiane-2-carboxylicacidethylester 97%
  • 1g
  • $ 30.00
  • Sigma-Aldrich
  • Ethyl 1,3-dithiane-2-carboxylate technical, ≥90% (GC)
  • 5ml
  • $ 244.00
  • Matrix Scientific
  • Ethyl 1,3-dithiane-2-carboxylate 98%
  • 10g
  • $ 202.00
  • Matrix Scientific
  • Ethyl 1,3-dithiane-2-carboxylate 98%
  • 5g
  • $ 133.00
  • Chem-Impex
  • Ethyl1,3-dithiane-2-carboxylate,≥98%(GC)Hazmat ≥98%(GC)
  • 1G
  • $ 30.05
Total 36 raw suppliers
Chemical Property of Ethyl 1,3-dithiane-2-carboxylate Edit
Chemical Property:
  • Appearance/Colour:Clear light yellow liquid. 
  • Vapor Pressure:0.0035mmHg at 25°C 
  • Melting Point:19-21°C 
  • Refractive Index:n20/D 1.539(lit.) 
  • Boiling Point:75-77 ºC (0.2 mmHg) 
  • Flash Point:130.2°C 
  • PSA:76.90000 
  • Density:1.22 
  • LogP:1.74570 
  • Storage Temp.:Store below +30°C. 
  • Water Solubility.:Slightly miscible with water. 
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:192.02787197
  • Heavy Atom Count:11
  • Complexity:132
Purity/Quality:

98%,99%, *data from raw suppliers

Ethyl 1,3-dithiane-2-carboxylate *data from reagent suppliers

Safty Information:
  • Pictogram(s): R10:; 
  • Hazard Codes:R10:; 
  • Statements: 10 
  • Safety Statements: 26-36/37/39-45 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CCOC(=O)C1SCCCS1
  • Uses Ethyl 1,3-dithiane-2-carboxylate is used in syn-selective aldol reactions. It undergoes asymmetric oxidation to give trans bis-sulfoxide. It is used to generate carbanon, which finds application in the preparation of alfa- keto esters.
Technology Process of Ethyl 1,3-dithiane-2-carboxylate

There total 5 articles about Ethyl 1,3-dithiane-2-carboxylate 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 boron trifluoride diethyl etherate; In chloroform; for 1.5h; Heating / reflux;
Guidance literature:
With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃; for 0.25h;
DOI:10.1016/j.tetlet.2006.12.066
Guidance literature:
With potassium carbonate; Aliquat 336; In toluene; for 8h; Ambient temperature;
Refernces Edit
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