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(R)-(+)-Trityl glycidyl ether

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(R)-(+)-Trityl glycidyl ether Basic information

Product Name:
(R)-(+)-Trityl glycidyl ether
Synonyms:
  • (R)-(+)-GLYCIDYL TRIPHENYLMETHYL ETHER
  • (R)-GLYCIDYL TRIPHENYLMETHYL ETHER
  • (R)-(+)-GLYCIDYL TRITYL ETHER
  • 2-[(triphenylmethyl)oxymethyl]oxirane
  • Trityl-(R)-glycidyl ether
  • (R)-GLYCIDYL TRITYL ETHER
  • (R)-2-(TRIPHENYLMETHOXYMETHYL)OXIRANE
  • (R)-2,3-EPOXY-1-PROPYL TRIPHENYLMETHYL ETHER
CAS:
65291-30-7
MF:
C22H20O2
MW:
316.39
EINECS:
1806241-263-5
Product Categories:
  • chiral
  • Heterocyclic Compounds
  • Chiral Building Blocks
  • Glycidyl Compounds, etc. (Chiral)
  • Oxiranes
  • Simple 3-Membered Ring Compounds
  • Synthetic Organic Chemistry
  • Chiral Building Blocks
  • Epoxides
  • Organic Building Blocks
Mol File:
65291-30-7.mol
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(R)-(+)-Trityl glycidyl ether Chemical Properties

Melting point:
99-102 °C (lit.)
alpha 
10.5 º (c=1 in chloroform)
Boiling point:
438.8±40.0 °C(Predicted)
Density 
1.146±0.06 g/cm3(Predicted)
storage temp. 
-20°C
solubility 
almost transparency in hot Methanol
form 
powder to crystal
color 
White to Almost white
optical activity
[α]20/D +10.5°, c = 1 in chloroform
CAS DataBase Reference
65291-30-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
37/39-26
WGK Germany 
3
HS Code 
2910.90.9100

MSDS

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(R)-(+)-Trityl glycidyl ether Usage And Synthesis

Chemical Properties

white to light yellow crystal powde

Uses

Nucleotides with activity against herpes simplex virus 1 and 2, lipid ammonium salts, and thio analogs of phospholipids have been prepared recently through ring-opening of this epoxide with cytosine derivatives, amines, and thiols, respectively.

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