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2-Propen-1-one, 1,1'-(4,6-dihydroxy-1,3-phenylene)bis[3-phenyl-, (E,E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84422-37-7

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84422-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84422-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,2 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84422-37:
(7*8)+(6*4)+(5*4)+(4*2)+(3*2)+(2*3)+(1*7)=127
127 % 10 = 7
So 84422-37-7 is a valid CAS Registry Number.

84422-37-7Relevant academic research and scientific papers

Bis-chalcone analogues as potent NO production inhibitors and as cytotoxic agents

Vijaya Bhaskar Reddy,Shen, Yuh-Chiang,Ohkoshi, Emika,Bastow, Kenneth F.,Qian, Keduo,Lee, Kuo-Hsiung,Wu, Tian-Shung

experimental part, p. 97 - 103 (2012/03/08)

Chalcones have a distinctive 1,3-diarylpropenone skeleton and exert numerous biological effects. Using a one-step Claisen-Schmidt condensation, we synthesized eleven bis-chalcones (3-13) and three acetyl chalcones (14-16) from substituted aldehydes and diacetylresorcinol. The compounds were tested for in vitro cytotoxic activity against four human cancer cell lines (A549, DU145, KB, and KB-VIN) and inhibition of NO production in lipopolysaccharide (LPS)-activated microglial cells. Among them, four compounds (3, 5, 6, and 13) showed significant cytotoxic activity with EC50 values ranging from 1.57 to 5.14 μM, and seven compounds (3, 5-8, 10, and 13) displayed potent anti-inflammatory activity by inhibiting NO production with IC50 values ranging from 0.95 to 8.65 μM. A mechanism of action study of active compounds 6 and 7 discovered that these compounds down-regulated iNOS expression by inhibiting p65 NF-κB activation/nuclear translocation due to prevention of IκBα degradation. Structure-activity relationship (SAR) findings are also discussed.

A facile synthesis of 3,7-diphenyl-4,6-distyryl-2,8-dioxo-2h,8h- benzo(1,2-b:5,4-b')dipyrans and their antifeedant activity

Sreenivasulu,Sarma

, p. 2281 - 2287 (2007/10/03)

The synthesis, characterisation and antifeedant activity of some new dicoumarins prepared from 4,6-diacetyl resorcinol has been reported.

Synthesis of 4,6-Bis(2'-substituted-2',3'-dihydro-1,5-benzothiazepin-4'-yl) resorcinols as potential antifeedants

Reddy, R Jayasimha,Ashok, D,Sarma, P N

, p. 404 - 406 (2007/10/02)

4,6-Bis(2'-substituted-2',3'-dihydro-1,5-benzothiazepin-4'-yl) resorcinols (3a-j) have been prepared in one step by the reaction of dichalcones (2a-j) with 2-aminothiophenol in ethanol containing gl. acetic acid and their structures established by element

Synthesis of Some Benzodipyrones from 4,6-Diacetylresorcinol

Anjaneyulu, A. S. R.,Mallavadhani, U. V.,Venkateswarlu, Y.

, p. 963 - 964 (2007/10/02)

Some α- and γ-benzodipyrones have been prepared in very good yield from 4,6-diacetylresorcinol (I) and characterised by their spectral data.

Homobiflavonoids from 5-Acetyl- and 3-Acetyl-resacetophenones

Mohan, Santosh Bala,Pal, Krishan,Murti, V. V. S.

, p. 714 - 717 (2007/10/02)

Reaction of 5- and 3-acetyl-resacetophenones with formaldehyde under acidic conditions yields the bis-methylene derivatives (V) and (XIa), respectively in good yields.These have been condensed with benzaldehyde to obtain the corresponding chalkones, which

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