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3-Pyridinemethanol, a-(4-fluorophenyl)-6-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

863443-00-9

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863443-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863443-00-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,4,4 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 863443-00:
(8*8)+(7*6)+(6*3)+(5*4)+(4*4)+(3*3)+(2*0)+(1*0)=169
169 % 10 = 9
So 863443-00-9 is a valid CAS Registry Number.

863443-00-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-fluorophenyl)[6-(methyloxy)-3-pyridinyl]methanol

1.2 Other means of identification

Product number -
Other names (4-fluorophenyl)[6-(methyloxy)-3-pyridinyl1]methanol

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:863443-00-9 SDS

863443-00-9Relevant academic research and scientific papers

A scaleable synthesis of methyl 3-amino-5-(4-fluorobenzyl)-2- pyridinecarboxylate

Boros, Eric E.,Burova, Svetlana A.,Erickson, Greg A.,Johns, Brian A.,Koble, Cecilia S.,Kurose, Noriyuki,Sharp, Matthew J.,Tabet, Elie A.,Thompson, James B.,Toczko, Matthew A.

, p. 899 - 902 (2007)

A scaleable synthesis of methyl 3-amino-5-(4-fluorobenzyl)-2- pyridinecarboxylate (1b), starting from 5-bromo-2-methoxypyridine (8) and 4-fluorobenzaldehyde (9), is described. Key steps in the process include lithium-bromine exchange of 8, addition of the

The Halogen–Samarium Exchange Reaction: Synthetic Applications and Kinetics

Anthore-Dalion, Lucile,Benischke, Andreas D.,Wei, Baosheng,Berionni, Guillaume,Knochel, Paul

supporting information, p. 4046 - 4050 (2019/02/26)

Fast I/Sm and Br/Sm exchanges take place when various aromatic or heterocyclic iodides and bromides are treated with nBu2SmCl?4 LiCl and nBu3Sm?5 LiCl, respectively. The resulting organosamarium reagents were efficiently quenched with aldehydes, ketones, and imines. Also, they undergo acylations when treated with N,N-dimethylamides leading to ketones. The rate of the Br/Sm exchange for a typical aryl bromide was determined and found to be 8.5×105 faster than the Br/Mg exchange, indicating that the rate of a metal-exchange is related to the ionic character of the carbon–metal bond and to the metal electronegativity.

HIV INTEGRASE INHIBITORS

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, (2015/09/22)

The present invention features compounds that are HIV integrase inhibitors and therefore are useful in the inhibition of HIV replication, the prevention and/or treatment of infection by HIV, and in the treatment of AIDS and/or ARC.

HIV INTEGRASE INHIBITORS

-

Page/Page column 49-50, (2008/06/13)

The present infention features compounds that are HIV integrase inhibitors and may be useful in the inhibition of HIV replication, the prevention and/or treatment of infection by HIV, and in the treatment of AIDS and/or ARC.

HIV INTEGRASE INHIBITORS

-

Page/Page column 36, (2010/11/26)

The present infention features compounds that are HIV integrase inhibitors and may be useful in the inhibition of HIV replication, the prevention and/or treatment of infection by HIV, and in the treatment of AIDS and/or ARC.

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