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(R)-(-)-GLYCIDYL1-NAPHTHYLETHER

Product Name
(R)-(-)-GLYCIDYL1-NAPHTHYLETHER
CAS No.
56715-28-7
Chemical Name
(R)-(-)-GLYCIDYL1-NAPHTHYLETHER
Synonyms
Ccris 6391;R-(-)-α-Naphthyl Glycidyl Ether;(R)-(-)-GLYCIDYL1-NAPHTHYLETHER;R-(-)-α-Naphthyl Glycidyl Ether;(R)-((1-Naphthalenyloxy)methyl)oxirane;(2R)-2-(Naphthalen-1-yloxymethyl)oxirane;Oxirane, ((1-naphthalenyloxy)methyl)-, (R)-;Oxirane, 2-[(1-naphthalenyloxy)methyl]-, (2R)-
CBNumber
CB31416991
Molecular Formula
C13H12O2
Formula Weight
200.23
MOL File
56715-28-7.mol
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(R)-(-)-GLYCIDYL1-NAPHTHYLETHER Property

storage temp. 
-20°C Freezer
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form 
Oil
color 
Colorless to Pale Yellow
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
N378390
Product name
R-(-)-α-NaphthylGlycidylEther
Packaging
250mg
Price
$95
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CCH0008329
Product name
(R)-(-)-GLYCIDYL1-NAPHTHYL ETHER
Purity
95.00%
Packaging
250MG
Price
$319.2
Updated
2021/12/16
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(R)-(-)-GLYCIDYL1-NAPHTHYLETHER Chemical Properties,Usage,Production

Chemical Properties

(R)-(-)-GLYCIDYL1-NAPHTHYLETHER is Colorless Oil

Uses

(R)-(-)-GLYCIDYL1-NAPHTHYLETHER used in the preparation of Naftopidil (N213500) enantiomers.

(R)-(-)-GLYCIDYL1-NAPHTHYLETHER Preparation Products And Raw materials

Raw materials

Preparation Products

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(R)-(-)-GLYCIDYL1-NAPHTHYLETHER Suppliers

Canada 1 China 9 India 2 United States 1 Global 13

56715-28-7, (R)-(-)-GLYCIDYL1-NAPHTHYLETHERRelated Search:

2-[(1-Naphthyloxy)methyl]oxirane Cladospirone bisepoxide kapurimycin A3 diepoxin sigma (R)-2-Oxiranylanisole (R)-(-)-GLYCIDYL1-NAPHTHYLETHER

  • (R)-(-)-GLYCIDYL1-NAPHTHYLETHER
  • (R)-((1-Naphthalenyloxy)methyl)oxirane
  • Ccris 6391
  • Oxirane, ((1-naphthalenyloxy)methyl)-, (R)-
  • R-(-)-α-Naphthyl Glycidyl Ether
  • Oxirane, 2-[(1-naphthalenyloxy)methyl]-, (2R)-
  • R-(-)-α-Naphthyl Glycidyl Ether
  • (2R)-2-(Naphthalen-1-yloxymethyl)oxirane
  • 56715-28-7
  • Aromatics
  • Chiral Reagents
  • Heterocycles
  • Intermediates