Cas 1357516-07-4,(Z)-4-(3,4,5-trimethoxybenzylidene)-2-phenyl-1H-imidazol-5(4H)-one

1357516-07-4

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Basic information

Product Name: (Z)-4-(3,4,5-trimethoxybenzylidene)-2-phenyl-1H-imidazol-5(4H)-one
Synonyms: (Z)-4-(3,4,5-trimethoxybenzylidene)-2-phenyl-1H-imidazol-5(4H)-one
CAS NO:1357516-07-4
Molecular Formula:
Molecular Weight: 338.363
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: (Z)-4-(3,4,5-trimethoxybenzylidene)-2-phenyl-1H-imidazol-5(4H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-4-(3,4,5-trimethoxybenzylidene)-2-phenyl-1H-imidazol-5(4H)-one(1357516-07-4)
EPA Substance Registry System: (Z)-4-(3,4,5-trimethoxybenzylidene)-2-phenyl-1H-imidazol-5(4H)-one(1357516-07-4)

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: 1357516-07-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1357516-07-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,5,1 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1357516-07:
(9*1)+(8*3)+(7*5)+(6*7)+(5*5)+(4*1)+(3*6)+(2*0)+(1*7)=164
164 % 10 = 4
So 1357516-07-4 is a valid CAS Registry Number.

1357516-07-4Upstream product

62616-09-5 (4Z)-2-phenyl-4-(3,4,5-trimethoxybenzylidene)-1,3-oxazol-5(4H)-one

1357516-07-4Downstream Products

1357516-07-4Relevant academic research and scientific papers

Efficient microwave-assisted synthesis and antioxidant activity of 4-arylidene-2-phenyl-1H-imidazol-5(4H)-ones

Shi, Feng,Zeng, Xiao-Ning,Wu, Fei-Yue,Yan, Shu,Zheng, Wei-Fa,Tu, Shu-Jiang

, p. 59 - 63 (2012)

The efficient synthesis of 4-arylidene-2-phenyl-1H-imidazol-5(4H)-ones was achieved via microwaveassisted reactions of 4-arylmethylene-2-phenyloxazol-5(4H) -ones with urea in glycol. This approach provides a facile shortcut for the synthesis of this type

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