Cas 84156-27-4,2-(2-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-(10H-phenothiazin-3-yl)-3,5-dihydro-imidazol-4-one

84156-27-4

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Basic information

Product Name: 2-(2-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-(10H-phenothiazin-3-yl)-3,5-dihydro-imidazol-4-one
Synonyms: 2-(2-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-(10H-phenothiazin-3-yl)-3,5-dihydro-imidazol-4-one
CAS NO:84156-27-4
Molecular Formula:
Molecular Weight: 554.467
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: 2-(2-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-(10H-phenothiazin-3-yl)-3,5-dihydro-imidazol-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-(10H-phenothiazin-3-yl)-3,5-dihydro-imidazol-4-one(84156-27-4)
EPA Substance Registry System: 2-(2-Bromo-phenyl)-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-3-(10H-phenothiazin-3-yl)-3,5-dihydro-imidazol-4-one(84156-27-4)

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: 84156-27-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 84156-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,5 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84156-27:
(7*8)+(6*4)+(5*1)+(4*5)+(3*6)+(2*2)+(1*7)=134
134 % 10 = 4
So 84156-27-4 is a valid CAS Registry Number.

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84156-27-4Relevant academic research and scientific papers

Imidazolines Containing Biologically Active Units: Part I- Synthesis of Imidazolines Containing Various Biologically Active Units

Sharief, A. M. Sh. El-,Harb, A.A.

, p. 449 - 453 (2007/10/02)

2-Aryl-4-arylidene-Δ2-oxazoline-5-ones (I) react with p-aminodiphenylamine to give 2-aryl-4-arylidene-1-(p-phenylaminophenyl)-Δ2-imidazolin-5-ones (II) which undergo cyclization with sulphur to the corresponding phenothiazine derivat

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