Cas 73043-24-0,(Z)-2-(4-(4-methoxybenzylidene)-2-methyl-5-oxo-4,5-dihihydro-1H-imidazol-1-yl)acetic acid

73043-24-0

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Basic information

Product Name: (Z)-2-(4-(4-methoxybenzylidene)-2-methyl-5-oxo-4,5-dihihydro-1H-imidazol-1-yl)acetic acid
Synonyms: (Z)-2-(4-(4-methoxybenzylidene)-2-methyl-5-oxo-4,5-dihihydro-1H-imidazol-1-yl)acetic acid
CAS NO:73043-24-0
Molecular Formula:
Molecular Weight: 274.276
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)-2-(4-(4-methoxybenzylidene)-2-methyl-5-oxo-4,5-dihihydro-1H-imidazol-1-yl)acetic acid(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-(4-(4-methoxybenzylidene)-2-methyl-5-oxo-4,5-dihihydro-1H-imidazol-1-yl)acetic acid(73043-24-0)
EPA Substance Registry System: (Z)-2-(4-(4-methoxybenzylidene)-2-methyl-5-oxo-4,5-dihihydro-1H-imidazol-1-yl)acetic acid(73043-24-0)

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: 73043-24-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 73043-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,4 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 73043-24:
(7*7)+(6*3)+(5*0)+(4*4)+(3*3)+(2*2)+(1*4)=100
100 % 10 = 0
So 73043-24-0 is a valid CAS Registry Number.

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73043-24-0Relevant academic research and scientific papers

Green fluorescent protein chromophore derivatives as a new class of aldose reductase inhibitors

Saito, Ryota,Hoshi, Maiko,Kato, Akihiro,Ishikawa, Chikako,Komatsu, Toshiya

, p. 965 - 974 (2016/10/25)

A number of (Z)-4-arylmethylene-1H-imidazol-5(4H)-ones, which are related to the fluorescent chromophore of the Aequorea green fluorescent protein (GFP), have been synthesized and evaluated their in vitro inhibitory activity against recombinant human aldo

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