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6B-Methoxy-3-Tropinon, also known as 6β-Methoxytropinone, is a chemical compound derived from tropinone, a key intermediate in the synthesis of various tropane alkaloids, which are naturally occurring compounds with significant pharmacological properties. This specific compound features a methoxy group at the 6β position, which can influence its reactivity and potential applications. It is often used in the synthesis of psychoactive substances and pharmaceuticals, highlighting its importance in the field of organic chemistry and drug development. However, due to its potential use in the illicit production of controlled substances, it is subject to regulatory controls and should be handled with caution and in accordance with applicable laws and safety protocols.

4839-12-7

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4839-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4839-12-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,3 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4839-12:
(6*4)+(5*8)+(4*3)+(3*9)+(2*1)+(1*2)=107
107 % 10 = 7
So 4839-12-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO2/c1-10-6-3-7(11)5-8(10)9(4-6)12-2/h6,8-9H,3-5H2,1-2H3/t6?,8?,9-/m1/s1

4839-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (6R)-6-methoxy-8-methyl-8-azabicyclo[3.2.1]octan-3-one

1.2 Other means of identification

Product number -
Other names 6exo-methoxy-tropan-3-one

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:4839-12-7 SDS

4839-12-7Relevant academic research and scientific papers

Synthesis and pharmacology of 6-substituted benztropines: Discovery of novel dopamine uptake inhibitors possessing low binding affinity to the dopamine transporter

Simoni, Daniele,Rossi, Marcello,Bertolasi, Valerio,Roberti, Marinella,Pizzirani, Daniela,Rondanin, Riccardo,Baruchello, Riccardo,Invidiata, Francesco Paolo,Tolomeo, Manlio,Grimaudo, Stefania,Merighi, Stefania,Varani, Katia,Gessi, Stefania,Borea, Pier Andrea,Marino, Silvia,Cavallini, Sabrina,Bianchi, Clementina,Siniscalchi, Anna

, p. 3337 - 3343 (2007/10/03)

A series of 6α- and 6β-substituted benztropines were synthesized. A marked enantioselectivity was observed for the 6β-methoxylated benztropines, the (1R)-isomers being more potent than the corresponding (1S) compounds. The racemic 6α-methoxy-3-(4′,4″- dif

Effects of two-carbon bridge region methoxylation of benztropine: Discovery of novel chiral ligands for the dopamine transporter

Simoni, Daniele,Roberti, Marinella,Rondanin, Riccardo,Baruchello, Riccardo,Rossi, Marcello,Invidiata, Francesco Paolo,Merighi, Stefania,Varani, Katia,Gessi, Stefania,Borea, Pier Andrea,Marino, Silvia,Cavallini, Sabrina,Bianchi, Clementina,Siniscalchi, Anna

, p. 823 - 827 (2007/10/03)

6-Methoxylated and 8-oxygenated benztropines were prepared and evaluated for their DAT and SERT activity (binding and uptake inhibition). Methoxylation at the two-carbon bridge of benztropine produced a novel class of potent and selective DAT ligands. An

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