Cas 97728-36-4,Acetamide, 2-chloro-N-[2-(4-hydroxy-1-oxo-3-phenyl-2(1H)-isoquinolinyl)phenyl]-

97728-36-4

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Basic information

Product Name: Acetamide, 2-chloro-N-[2-(4-hydroxy-1-oxo-3-phenyl-2(1H)-isoquinolinyl)phenyl]-
Synonyms:
CAS NO:97728-36-4
Molecular Formula: C23H17ClN2O3
Molecular Weight: 404.853
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: Acetamide, 2-chloro-N-[2-(4-hydroxy-1-oxo-3-phenyl-2(1H)-isoquinolinyl)phenyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Acetamide, 2-chloro-N-[2-(4-hydroxy-1-oxo-3-phenyl-2(1H)-isoquinolinyl)phenyl]-(97728-36-4)
EPA Substance Registry System: Acetamide, 2-chloro-N-[2-(4-hydroxy-1-oxo-3-phenyl-2(1H)-isoquinolinyl)phenyl]-(97728-36-4)

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: 97728-36-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 97728-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,7,2 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97728-36:
(7*9)+(6*7)+(5*7)+(4*2)+(3*8)+(2*3)+(1*6)=184
184 % 10 = 4
So 97728-36-4 is a valid CAS Registry Number.

97728-36-4Upstream product

97728-36-4Downstream Products

97728-37-5 2-Chloro-N-[2-(1,4-dioxo-3-phenyl-3,4-dihydro-1H-isoquinolin-2-yl)-phenyl]-acetamide

97728-36-4Relevant academic research and scientific papers

KETO-ENOL TAUTOMERISM OF 4-HYDROXY-3-PHENYL-2-(2-CHLOROACETAMIDOPHENYL)-1-ISOQUINOLONE

Valter, R. E.,Batse, A. E.,Valtere, S. P.

, p. 453 - 454 (2007/10/02)

Three crystalline modifications of the N-chloroacetyl derivative were obtained in the chloroacetylation of 2-(2-aminophenyl)-4-hydroxy-3-phenyl-1-isoquinolone.It was established by IR spectroscopy that they differ with respect to isomeric composition and

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