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931409-24-4

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931409-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 931409-24-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,1,4,0 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 931409-24:
(8*9)+(7*3)+(6*1)+(5*4)+(4*0)+(3*9)+(2*2)+(1*4)=154
154 % 10 = 4
So 931409-24-4 is a valid CAS Registry Number.

931409-24-4SDS

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 5-[3-(3-hydroxyphenoxy)azetidin-1-yl]-5-methyl-2,2-diphenylhexanamide

1.2 Other means of identification

Product number -
Other names UNII-O0RG3QM34H

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:931409-24-4 SDS

931409-24-4Relevant academic research and scientific papers

Development of a scaleable synthesis of a geminal dimethyl tertiary amine as an inhaled muscarinic antagonist for the treatment of COPD

Dillon, Barry R.,Roberts, Dannielle F.,Entwistle, David A.,Glossop, Paul A.,Knight, Craig J.,Laity, Daniel A.,James, Kim,Praquin, Celine F.,Strang, Ross S.,Watson, Christine A. L.

, p. 195 - 203 (2012/06/05)

An efficient and scalable process for the synthesis of muscarinic antagonist, PF-3635659 1, is described, illustrating redesign of an analogue-targeted synthesis which contained a scale-limiting rhodium-activated C-H amination step. The final route includes a reproducible modified Bouveault reaction which has not previously been reported on a substrate of this complexity, or on such a scale with over 5 kg of the requisite gem-dimethylamine prepared via this methodology.

Inhalation by design: Novel tertiary amine muscarinic M3 receptor antagonists with slow off-rate binding kinetics for inhaled once-daily treatment of chronic obstructive pulmonary disease

Glossop, Paul A.,Watson, Christine A. L.,Price, David A.,Bunnage, Mark E.,Middleton, Donald S.,Wood, Anthony,James, Kim,Roberts, Dannielle,Strang, Ross S.,Yeadon, Michael,Perros-Huguet, Christelle,Clarke, Nicholas P.,Trevethick, Michael A.,MacHin, Ian,Stuart, Emilio F.,Evans, Steven M.,Harrison, Anthony C.,Fairman, David A.,Agoram, Balaji,Burrows, Jane L.,Feeder, Neil,Fulton, Craig K.,Dillon, Barry R.,Entwistle, David A.,Spence, Fiona J.

, p. 6888 - 6904 (2011/12/03)

A novel tertiary amine series of potent muscarinic M3 receptor antagonists are described that exhibit potential as inhaled long-acting bronchodilators for the treatment of chronic obstructive pulmonary disease. Geminal dimethyl functionality pr

HYDROCHLORIDE SALT OF 5-R3-F3-TIVDROXYPHENOXY)AZETIDIπ-1-Vπ-5-METHYL-2.2- DIPHENYLHEXANAMIDE

-

Page/Page column 14; 15, (2009/01/20)

This invention relates to the hydrochloride salt of 5-[3-{3-hydroxyphenoxy)azetidin-1-yl]-5- methyl-2,2-diphenylhexanamide or derived form thereof and its use as a medicament.

CARBOXAMIDE DERIVATIVES AS MUSCARINIC RECEPTOR ANTAGONISTS

-

Page/Page column 129, (2008/06/13)

The invention relates to compounds of Formula (I) processes and intermediates for their preparation, their use as muscarinic antagonists and pharmaceutical composition containing them.

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