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(+/-)-5-hydroxy-7-(4'-hydroxyphenyl)-1-phenyl-3-heptanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83161-96-0

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83161-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83161-96-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,6 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83161-96:
(7*8)+(6*3)+(5*1)+(4*6)+(3*1)+(2*9)+(1*6)=130
130 % 10 = 0
So 83161-96-0 is a valid CAS Registry Number.

83161-96-0Downstream Products

83161-96-0Relevant academic research and scientific papers

Antiviral activity of diarylheptanoid stereoisomers against respiratory syncytial virus in vitro and in vivo

Konno, Katsuhiko,Miura, Motofumi,Toriyama, Masaharu,Motohashi, Shigeyasu,Sawamura, Rie,Watanabe, Wataru,Yoshida, Hiroki,Kato, Masahiko,Yamamoto, Ryuichi,Yasukawa, Ken,Kurokawa, Masahiko

, p. 773 - 781 (2013)

We previously showed that (5S)-5-hydroxy-7-(4-hydroxyphenyl)-1-phenylhept- 3-one (AO-0011) and (5S)-5-methoxy-1,7-diphenylhept-3-one (AO-0016) isolated from Alpinia officinarum exhibited stronger anti-influenza virus activity and anti-respiratory syncytia

Synthesis and digestibility inhibition of diarylheptanoids: Structure- activity relationship

Bratt, Katharina,Sunnerheim, Kerstin

, p. 2703 - 2713 (2007/10/03)

(±)-5-Hydroxy-1,7-bis-(4'-hydroxyphenyl)-3-heptanone (2a), (±)5- hydroxyl-1-(4'-hydroxyphenyl)-7-phenyl-3-heptanone (2b), (±)-5-hydroxy-7- (4'-hydroxyphenyl)-1-phenyl-3-heptanone (2c), and (±)-5-hydroxy-1,7- bis(phenyl)-3-heptanone (2d) have been synthesized to study the structure- activity relationship regarding digestibility inhibition in vitro in cow rumen fluid. The activities were compared with the activity of chiral (S)-2a and its glucoside platyphylloside (1), isolated from Betula pendula. Compound 2a was slightly less active, 2b and 2c were more active, and 2d was less active than (S)-2a and platyphylloside.

NEW METHODS AND REAGENTS IN ORGANIC SYNTHESIS. 47. A GENERAL, EFFICIENT, AND CONVENIENT SYNTHESIS OF DIARYLHEPTANOIDS

Kato, Nobuharu,Hamada, Yasumasa,Shioiri, Takayuki

, p. 3323 - 3326 (2007/10/02)

An efficient synthesis of physiologically interesting diarylheptanoids has been carried out through direct C-acylation using diethyl phosphorocyanidate (DEPC) followed by Grignard reactions with aldehydes.Keywords - diarylheptanoid; C-acylation; diethyl p

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