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CC1C=C(C(Cl)=CC=1OC)C1N=C(SC=1C)N(CC#C)C(CC1CC1)C1C=C(F)C(C)=CC=1
InChi: InChI=1S/C37H42FN7O10/c1-53-32(47)13-12-27(34(49)44-30(15-24-19-39-21-41-24)36(51)43-28(31(46)17-38)16-33(48)54-2)42-35(50)29(14-23-18-40-26-11-7-6-10-25(23)26)45-37(52)55-20-22-8-4-3-5-9-22/h3-11
with an EC50 of 1 nM
Smiles: NS(=O)(=O)C1C=CC(=CC=1)N1N=C(CCCNC(=O)NC2C=CC(=CC=2)C(F)(F)F)C=C1C1C=CC=CC=1
InChiKey: VLGATXOTCNBWIT-UHFFFAOYSA-N
trans-Cinnamaldehyde uinoline quinone CC1C=C(C(Cl)=CC=1OC)C1N=C(SC=1C)N(CC#C)C(CC1CC1)C1C=C(F)C(C)=CC=1trans Cinnamaldehyde can be used to prepare highly polyfunctionalized furan ring by reaction of alkyl isocyanides with dialkyl acetylenedicarboxylate. trans Cinnamaldehyde can be used to synthesize trans cinnamaldehyde cyclodextrin complex, an antimicrobial edible coating that increases the shelf life of fresh cut fruits. Product information CAS Number: 14371 10 9 Molecular Weight: 132. 16 Formula: C9H8O Chemical Name: (2E) 3 phenylprop 2 enal Smiles:
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