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6-fluoro-6-desoxyoxymorphone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92593-44-7

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92593-44-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92593-44-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,9 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92593-44:
(7*9)+(6*2)+(5*5)+(4*9)+(3*3)+(2*4)+(1*4)=157
157 % 10 = 7
So 92593-44-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H20FNO3/c1-19-7-6-16-13-9-2-3-11(20)14(13)22-15(16)10(18)4-5-17(16,21)12(19)8-9/h2-3,10,12,15,20-21H,4-8H2,1H3/t10-,12-,15+,16+,17-/m1/s1

92593-44-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R,4aS,7R,7aR,12bS)-7-fluoro-3-methyl-1,2,4,5,6,7,7a,13-octahydro-4,12-methanobenzofuro[3,2-e]isoquinoline-4a,9-diol

1.2 Other means of identification

Product number -
Other names 6-Fluoro-6-desoxyoxymorphone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:92593-44-7 SDS

92593-44-7Downstream Products

92593-44-7Relevant academic research and scientific papers

Probes for narcotic receptor mediated phenomena. 11. Synthesis of 17-methyl and 17-cyclopropylmethyl-3,14-dihydroxy-4,5α-epoxy-6β-fluoromorphinans (foxy and cyclofoxy) as model of opioid ligands suitable for positron emission transaxial tomography

Burke, Terrence R.,Rice, Kenner C.,Pert, Candace B.

, p. 99 - 106 (2007/10/02)

Fluorinated derivatives 3,14-dihydroxy-4,5α-epoxy-6β-fluoro-17-methylmorphinan ("fluorooxymorphone": FOXY, 10) and 17-cyclopropylmethyl-3,14-dihydroxy-4,5α-epoxy-6β-fluoromorphnian (CYCLOFOXY, 18) were prepared based upon the structures of the potent opioid agonist oxymorphone 4 and the antagonist naltrexone 11 respectively.Fluorine was introduced in the final stages of synthesis by a facile nucleophilic displacement with fluoride ion of the 6α-triflate functions in 8 and 16.The synthetic procedures are suitable for the production of the corresponding positron emitting 18F-labeled analogs 18F-FOXY and 18F-CYCLOFOXY, which may be usefuf for in vivo studies of the opioid receptor system using positron emission transaxial tomography.In addition, the tritiation of FOXY (10) to high specific activity is described

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