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S-(+)-α-Naphthyl Glycidyl Ether

Product Name
S-(+)-α-Naphthyl Glycidyl Ether
CAS No.
61249-00-1
Chemical Name
S-(+)-α-Naphthyl Glycidyl Ether
Synonyms
Ccris 6392;S-(+)-α-Naphthyl Glycidyl Ether;S-(+)-α-Naphthyl Glycidyl Ether;(S)-(+)-GLYCIDYL1-NAPHTHYLETHER;(S)-((1-Naphthalenyloxy)methyl)oxirane;(2S)-2-(Naphthalen-1-yloxymethyl)oxirane;Oxirane, ((1-naphthalenyloxy)methyl)-, (S)-;Oxirane, 2-[(1-naphthalenyloxy)methyl]-, (2S)-
CBNumber
CB41251452
Molecular Formula
C13H12O2
Formula Weight
200.23
MOL File
61249-00-1.mol
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S-(+)-α-Naphthyl Glycidyl Ether Property

storage temp. 
-20°C Freezer
solubility 
Chloroform (Slightly), Methanol (Sparingly)
form 
Oil
color 
Clear Colourless
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
N378395
Product name
S-(+)-α-NaphthylGlycidylEther
Packaging
100mg
Price
$175
Updated
2021/12/16
TRC
Product number
N378395
Product name
S-(+)-α-NaphthylGlycidylEther
Packaging
1g
Price
$1355
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CCH0008345
Product name
OXIRANE, ((1-NAPHTHALENYLOXY)METHYL)-, (S)-
Purity
95.00%
Packaging
5MG
Price
$497.77
Updated
2021/12/16
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S-(+)-α-Naphthyl Glycidyl Ether Chemical Properties,Usage,Production

Chemical Properties

S-(+)-α-Naphthyl Glycidyl Ether is Colorless Oil

Uses

S-(+)-α-Naphthyl Glycidyl Ether is used in the preparation of Naftopidil (N213500) enantiomers.

S-(+)-α-Naphthyl Glycidyl Ether Preparation Products And Raw materials

Raw materials

Preparation Products

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S-(+)-α-Naphthyl Glycidyl Ether Suppliers

J & K SCIENTIFIC LTD.
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010-82848833 400-666-7788
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Ningbo Zhenyue Pharmaceutical Technology Co., Ltd
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61249-00-1, S-(+)-α-Naphthyl Glycidyl EtherRelated Search:


  • Oxirane, ((1-naphthalenyloxy)methyl)-, (S)-
  • (S)-(+)-GLYCIDYL1-NAPHTHYLETHER
  • (S)-((1-Naphthalenyloxy)methyl)oxirane
  • Ccris 6392
  • S-(+)-α-Naphthyl Glycidyl Ether
  • Oxirane, 2-[(1-naphthalenyloxy)methyl]-, (2S)-
  • (2S)-2-(Naphthalen-1-yloxymethyl)oxirane
  • S-(+)-α-Naphthyl Glycidyl Ether
  • 61249-00-1
  • Heterocycles
  • Intermediates
  • Aromatics
  • Chiral Reagents