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2-Oxazolidinone, 3-[6-(3-butenyloxy)hexyl]-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-, (5R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

686351-12-2

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686351-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 686351-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,6,3,5 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 686351-12:
(8*6)+(7*8)+(6*6)+(5*3)+(4*5)+(3*1)+(2*1)+(1*2)=182
182 % 10 = 2
So 686351-12-2 is a valid CAS Registry Number.

686351-12-2Relevant academic research and scientific papers

Discovery of a rapidly metabolized, long-acting β2 adrenergic receptor agonist with a short onset time incorporating a sulfone group suitable for once-daily dosing

Procopiou, Panayiotis A.,Barrett, Victoria J.,Biggadike, Keith,Butchers, Peter R.,Craven, Andrew,Ford, Alison J.,Guntrip, Stephen B.,Holmes, Duncan S.,Hughes, Sara C.,Jones, Anne E.,Looker, Brian E.,Mutch, Peter J.,Ruston, Mark,Needham, Deborah,Smith, Claire E.

supporting information, p. 159 - 170 (2014/02/14)

A series of novel, potent, and selective human β2 adrenoceptor agonists incorporating a sulfone moiety on the terminal right-hand-side phenyl ring of (R)-salmeterol is presented. Sulfone 10b had salmeterol-like potency and selectivity profile, long duration of action on guinea pig trachea, and longer than salmeterol duration of action in vivo, suitable for once-daily dosing. It had lower than salmeterol oral absorption in rat, lower bioavailability in rat and dog, and a high turnover in human hepatocytes. It was metabolized in human hepatocytes by hydroxylation, oxidation, cleavage, and conjugation; most of the metabolites would be expected to have reduced or no β2 activity. The 4-biphenylsulfonic acid was identified as a crystalline, non-hygroscopic salt of 10b, suitable for inhaled delivery. Furthermore, it was free of any genetic toxicity issues and was considered as a backup to vilanterol.

PHENETHANOLAMINE DERIVATIVE FOR THE TREATMENT OF RESPIRATORY DISEASES

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Page 53-54, (2010/02/06)

The present invention relates to novel compounds of formula (I), to a process for their manufacture, to pharmaceutical compositions containing them, and to their use in therapy, in particular their use in the prophylaxis and treatment of respiratory diseases.

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