Cas 1412410-76-4,(E)-3-(7-Methoxy-4-oxo-4H-chromen-3-yl)-N-phenylacrylamide

1412410-76-4

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Basic information

Product Name: (E)-3-(7-Methoxy-4-oxo-4H-chromen-3-yl)-N-phenylacrylamide
Synonyms: (E)-3-(7-Methoxy-4-oxo-4H-chromen-3-yl)-N-phenylacrylamide
CAS NO:1412410-76-4
Molecular Formula:
Molecular Weight: 321.332
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: (E)-3-(7-Methoxy-4-oxo-4H-chromen-3-yl)-N-phenylacrylamide(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3-(7-Methoxy-4-oxo-4H-chromen-3-yl)-N-phenylacrylamide(1412410-76-4)
EPA Substance Registry System: (E)-3-(7-Methoxy-4-oxo-4H-chromen-3-yl)-N-phenylacrylamide(1412410-76-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1412410-76-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1412410-76-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,2,4,1 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1412410-76:
(9*1)+(8*4)+(7*1)+(6*2)+(5*4)+(4*1)+(3*0)+(2*7)+(1*6)=104
104 % 10 = 4
So 1412410-76-4 is a valid CAS Registry Number.

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1412410-76-4Relevant academic research and scientific papers

Heck cross-coupling reactions in ionic liquid mediated pd nanocatalysts

Gautam, Prashant,Srivastava, Vivek

, p. 359 - 372 (2021/09/07)

We straightforwardly synthesized 18 different types of palladium nanoparticles by using a series of palladium metal precursors and ionic liquids. All the materials went for XRD, TEM, and ICP-OES analysis, before going to Heck cross-coupling reaction as a catalyst. We evaluated the catalytic performance of our developed IL#Pd MNP catalyst over Heck cross-coupling reaction between different terminal olefins with various 3-iodo-benzopyrones, including sterically hindered, electron-rich, electron neutral and electron-deficient systems. We obtained the Heck cross-coupling reaction product in good to average yield under phosphine free reaction condition with an added advantage of 6 times catalyst recycling.

Anti-hepatitis B virus and anti-cancer activities of novel isoflavone analogs

Zhang, Yikai,Zhong, Hanyu,Lv, Zhiliang,Zhang, Mingfeng,Zhang, Tao,Li, Qisheng,Li, Ke

, p. 158 - 167 (2013/05/09)

We have synthesized a series of novel isoflavone analogs and evaluated their anti-HBV and anti-cancer activities in vitro. The bioassays showed that the majority of the resultant compounds exerted inhibitory effects on HBsAg and HBeAg levels, HBV DNA replication, as well as the growth of four human cancer cell lines to various extents, which supported the rationale of the design. In particular, compound 8f showed the highest activity against HBV infection and HBV-related liver cancer. Compound 7l (IC50 = 0.47 μM) also exerted remarkable inhibitory effect on the growth lung cancer cell line A-549.

Efficient Heck cross-coupling of 3-iodo-benzopyrones with olefins under microwave irradiation without phosphine

Zhang, Yikai,Lv, Zhiliang,Zhong, Hanyu,Zhang, Mingfeng,Zhang, Tao,Zhang, Wannian,Li, Ke

, p. 9777 - 9787 (2012/11/07)

An efficient and effective microwave-assisted Heck cross-coupling of different terminal olefins with various 3-iodo-benzopyrones including sterically hindered, electron-rich, electron-neutral, and electron-deficient is developed. It proceeded faster and g

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