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(S)-(-)-Trityl glycidyl ether

Base Information Edit
  • Chemical Name:(S)-(-)-Trityl glycidyl ether
  • CAS No.:129940-50-7
  • Molecular Formula:C22H20O2
  • Molecular Weight:316.4
  • Hs Code.:29109000
  • DSSTox Substance ID:DTXSID50428235
  • Nikkaji Number:J1.389.667D
  • Wikidata:Q72515552
  • Mol file:129940-50-7.mol
(S)-(-)-Trityl glycidyl ether

Synonyms:(S)-(-)-Glycidyl trityl ether;(S)-2-[(Trityloxy)methyl]oxirane;(S)-O-Tritylglycidol;(S)-Trityloxymethyloxirane;Trityl (S)-glycidyl ether;Oxirane,[(triphenylmethoxy)methyl]-, (2S)- (9CI);Oxirane, [(triphenylmethoxy)methyl]-,(S)-;(R)-Glycidol trityl ether;

Suppliers and Price of (S)-(-)-Trityl glycidyl ether
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
  • (S)-(-)-TritylGlycidylEther
  • 50mg
  • $ 45.00
  • TCI Chemical
  • (S)-Glycidyl Trityl Ether >98.0%(GC)
  • 5g
  • $ 74.00
  • TCI Chemical
  • (S)-Glycidyl Trityl Ether >98.0%(GC)
  • 25g
  • $ 222.00
  • SynQuest Laboratories
  • (2S)-2-[(Trityloxy)methyl]oxirane 98%
  • 100 g
  • $ 472.00
  • SynQuest Laboratories
  • (2S)-2-[(Trityloxy)methyl]oxirane 98%
  • 25 g
  • $ 128.00
  • Sigma-Aldrich
  • (S)-(?)-Glycidyl trityl ether 98%
  • 5g
  • $ 137.00
  • Frontier Specialty Chemicals
  • (S)-Glycidyl Trityl Ether 98%
  • 1g
  • $ 26.00
  • Crysdot
  • (S)-2-((Trityloxy)methyl)oxirane 98%
  • 25g
  • $ 104.00
  • Chem-Impex
  • (S)-Glycidyltritylether,98%(Chiralpurity,GC) 98%(Chiralpurity,GC)
  • 5G
  • $ 118.72
  • Chem-Impex
  • (S)-Glycidyltritylether,98%(Chiralpurity,GC) 98%(Chiralpurity,GC)
  • 25G
  • $ 445.76
Total 76 raw suppliers
Chemical Property of (S)-(-)-Trityl glycidyl ether Edit
Chemical Property:
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:1.73E-07mmHg at 25°C 
  • Melting Point:99-102 °C(lit.) 
  • Refractive Index:-11 ° (C=1, CHCl3) 
  • Boiling Point:438.8 °C at 760 mmHg 
  • Flash Point:164.8 °C 
  • PSA:21.76000 
  • Density:1.146 g/cm3 
  • LogP:4.39390 
  • Storage Temp.:under inert gas (nitrogen or Argon) at 2-8°C 
  • Solubility.:almost transparency in hot Methanol 
  • XLogP3:4.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:6
  • Exact Mass:316.146329876
  • Heavy Atom Count:24
  • Complexity:330
Purity/Quality:

98%,99%, *data from raw suppliers

(S)-(-)-TritylGlycidylEther *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 37/39-26 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C1C(O1)COC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4
  • Isomeric SMILES:C1[C@H](O1)COC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4
  • Uses (S)-(-)-Glycidyl trityl ether may be used to prepare N-(p-alkoxy)benzoyl-2-methylindole-4-acetic acid analogs, which are potent prostaglandin D2 (PGD2) receptor antagonists. It may also be used as a starting material in the multi-step synthesis of (-)-actisonitrile.
Technology Process of (S)-(-)-Trityl glycidyl ether

There total 9 articles about (S)-(-)-Trityl glycidyl ether 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 dmap; triethylamine; In dichloromethane; at 25 ℃; for 24h;
DOI:10.1055/s-2007-990883
Guidance literature:
With triethylamine; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1055/s-0029-1218665
Guidance literature:
With water; In dichloromethane; acetonitrile; at 0 - 20 ℃; Resolution of racemate;
DOI:10.1021/ja302340b
Refernces Edit
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