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3-(2-chloro-4-fluorophenoxy)-N-(6-methoxypyridin-3-yl)azetidine-1-carbothioamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

900512-30-3

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900512-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 900512-30-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,0,5,1 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 900512-30:
(8*9)+(7*0)+(6*0)+(5*5)+(4*1)+(3*2)+(2*3)+(1*0)=113
113 % 10 = 3
So 900512-30-3 is a valid CAS Registry Number.

900512-30-3Downstream Products

900512-30-3Relevant academic research and scientific papers

Triazole oxytocin antagonists: Identification of an aryloxyazetidine replacement for a biaryl substituent

Brown, Alan,Brown, T. Bruce,Calabrese, Andrew,Ellis, Dave,Puhalo, Nicholas,Ralph, Michael,Watson, Lesa

scheme or table, p. 516 - 520 (2010/04/05)

A series of aryloxyazetidines, aryloxypyrrolidines and aryloxypiperidines were designed based on structural overlap with previously reported arylpyrazine Oxytocin antagonists. Similarly high levels of Oxytocin antagonism were achievable in these new serie

A convenient synthesis of highly substituted 3-N,N-dialkylamino-1,2,4- triazoles

Batchelor, David V.,Beal, David M.,Brown, T. Bruce,Ellis, David,Gordon, David W.,Johnson, Patrick S.,Mason, Helen J.,Ralph, Michael J.,Underwood, Toby J.,Wheeler, Simon

scheme or table, p. 2421 - 2424 (2009/04/08)

The title compounds are prepared from S-methylisothioureas and acyl hydrazides in moderate to good yields. The reaction is characterized by relatively mild conditions and very broad functional group tolerance. Georg Thieme Verlag Stuttgart.

Substituted triazole derivatives as oxytocin antagonists

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Page/Page column 38, (2008/06/13)

The present invention relates to substituted triazoles of formula (I), uses thereof, processes for the preparation thereof and compositions containing said compounds. These inhibitors have utility in a variety of therapeutic areas including sexual dysfunction.

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