Cas 113735-23-2,3,4-dimethoxy-2'-hydroxy-3',4'-methylenedioxychalcone

113735-23-2

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Basic information

Product Name: 3,4-dimethoxy-2'-hydroxy-3',4'-methylenedioxychalcone
Synonyms: 3,4-dimethoxy-2'-hydroxy-3',4'-methylenedioxychalcone
CAS NO:113735-23-2
Molecular Formula:
Molecular Weight: 328.321
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3,4-dimethoxy-2'-hydroxy-3',4'-methylenedioxychalcone(CAS DataBase Reference)
NIST Chemistry Reference: 3,4-dimethoxy-2'-hydroxy-3',4'-methylenedioxychalcone(113735-23-2)
EPA Substance Registry System: 3,4-dimethoxy-2'-hydroxy-3',4'-methylenedioxychalcone(113735-23-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 113735-23-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 113735-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,3 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113735-23:
(8*1)+(7*1)+(6*3)+(5*7)+(4*3)+(3*5)+(2*2)+(1*3)=102
102 % 10 = 2
So 113735-23-2 is a valid CAS Registry Number.

113735-23-2Upstream product

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113735-23-2Relevant academic research and scientific papers

Methylenedioxy flavonoids: Assessment of cytotoxic and anti-cancer potential in human leukemia cells

Orlikova, Barbora,Menezes, José C.J.M.D.S.,Ji, Seungwon,Kamat, Shrivallabh P.,Cavaleiro, José A.S.,Diederich, Marc

, p. 173 - 180 (2014/07/22)

A new series of chalcones, flavanones and flavones with methylenedioxy group at the 3,4 position in chalcone, 7,8 position in flavanones and flavones with mono-, di- and trimethoxy groups in the benzaldehyde ring have been assessed for their effect on pro

Electrospray tandem mass spectrometry analysis of methylenedioxy chalcones, flavanones and flavones

Menezes, José C. J. M. D. S.,Cavaleiro, José A. S.,Kamat, Shrivallabh P.,Barros, Cristina M. R. F.,Domingues, M. Rosário M.

, p. 1303 - 1310 (2013/07/28)

RATIONALE Several methylenedioxy chalcones, flavanones and flavones substituted with mono-, di- and trimethoxy groups have been used in the treatment of proliferative conditions like cancer and inflammatory diseases. The application of these flavonoids in

13C Nuclear Magnetic Resonance Studies on 1,3-Diphenylprop-2-enones

Parmar, V. S.,Sharma, Sunil,Rathore, J. S.,Garg, Meenu,Gupta, Sandhya,et al.

, p. 470 - 474 (2007/10/02)

The 13C NMR spectra of 48 differently substituted chalcones (1,3-diphenylprop-2-enones) have been recorded and the results are discussed.The data will be useful in the identification of new/natural chalcones.

Synthesis of a New Isoflavone Occuring in Tephrosia maxima (Pers)

Parmar, V. S.,Singh, Suddham,Jain, Rajni

, p. 484 - 485 (2007/10/02)

7,8-Methylenedioxy-3',4'-dimethoxyisoflavone (I), a new isoflavone isolated from the aerial parts and roots of Tephrosia maxima has been synthesized by oxidative rearrangement of 2'-hydroxy-3',4'-methylenedioxy-3,4-dimethoxychalcone (IV) with thallium(III) nitrate (TTN) in trimethyl orthoformate (TMOF), followed by acid-catalysed cyclization.It has also been synthesized from 2,3,4-trihydroxy-3',4'-dimethoxydeoxybenzoin (V).

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