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Catalogue
Number
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Product
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Order number / Unit
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1900
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MMSE
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1900.0001: 1 mg per vial
1900.0002: 2 mg per vial
Please inquire for customized
filling and bulk quantities.
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Precursor for 16alpha-[18F]Fluoroestradiol
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Molar Mass: 394.48
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C20H26O6S
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[177714-21-5]
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Nearly colourless crystals packaged in dark glass crimp cap vials.
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Purity: > 95 %
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Certificates:
CoA; 1H and 13C NMR spectra
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Chemical Name:
CA index name: Estra-1,3,5(10)-triene-16,17-diol, 3-(methoxymethoxy)-, cyclic sulfate, (16beta,17beta)
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Synonymes:
3-(Methoxymethoxy)-1,3,5(10)-gonatriene-16beta,17beta diol-16,17-cyclic sulfate; 3-O-(Methoxymethyl)-16,17-O-sulfuryl-16-epiestriol; 3-Methoxymethyl-16beta,17beta-epiestriol-O-cyclic sulfone; FES precursor
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Literature:
1. Roemer J. et al. Automated production of n.c.a. 16alpha-[18F]fluoroestradiol. Forschungszent. Rossendorf, [Ber.] FZR 1997, 200, 188-192.
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2. Lim J.L. et al. The use of 3-methoxymethyl-16alpha,17beta-epiestriol-O-cyclic sulfone as the precursor in the synthesis of [18F]-16alpha-fluoroestradiol. Nucl. Med. Biol. 1996, 23, 911-915.
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3. Roemer J. et al. 13C NMR spectroscopic characterization of estra-1,3,5(10)-triene-3,17beta-diol and 3,16,17-triols, and some of their 3-O-methoxymethyl and 16alpha-fluoro derivatives. Forschungszent. Rossendorf, [Ber.] FZR 1996, 122, 27-30.
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4. Berridge M.S. et al. Cyclic sulfates: useful substrates for selective nucleophilic substitution. J. Org. Chem. 1990, 55, 1211-1217.
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date of product catalogue issue:
05 April 2012
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