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4'-<<3-butyl-5,6-dihydro-5-oxo-6-(phenylethyl)-4H-1,2,4-oxadiazin-4-yl>methyl><1,1'-biphenyl>-2-carboxylic acid t-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

150694-40-9

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150694-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150694-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,6,9 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 150694-40:
(8*1)+(7*5)+(6*0)+(5*6)+(4*9)+(3*4)+(2*4)+(1*0)=129
129 % 10 = 9
So 150694-40-9 is a valid CAS Registry Number.

150694-40-9Relevant academic research and scientific papers

SYNTHESIS OF N-ALKYL-1,2,4-OXADIAZINONES AS ANGIOTENSIN-II (AT1) RECEPTOR ANTAGONISTS

Weller, Harold N.,Miller, Arthur V.,Dickinson, Kenneth E.,Hedberg, S. Anders,Delaney, Carol L.,et al.

, p. 1027 - 1038 (2007/10/02)

4-Alkyl-1,2,4-oxadiazinones were prepared by regiospecific alkylation of the corresponding 4H-oxadiazinones, which were synthesized by a trimethylaluminium mediated cyclization reaction.Alkylation was regiospecyfic and generally facile; in one example, however, an unusual fragmentation reaction occurred.A homochiral oxadiazineone was also prepared and alkylated under the described conditions. 4-Biphenylmethyl-1,2,4-oxadi-azinones were potent angiotensin-II receptor antagonists.

BIPHENYL OXADIAZINONE ANGIOTENSIN II INHIBITORS

-

, (2008/06/13)

Angiotension II inhibition is exhibited by STR1 wherein: R. sup.1 and R 2 are each independently hydrogen, alkyl, aryl, aralkyl, cycloalkyl, cycloalkylalkyl, thiophenalkyl, pyridylalkyl, or--R 8 CO. sub.2 R 9 ;R 3 is a single bond,--S--, or--O--;

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