Cas 881192-18-3,2(1H)-Pyridinone, 3-acetyl-6-(1-methylethyl)-5-(3-methyl-5-isoxazolyl)-4-phenyl-

881192-18-3

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Basic information

Product Name: 2(1H)-Pyridinone, 3-acetyl-6-(1-methylethyl)-5-(3-methyl-5-isoxazolyl)-4-phenyl-
Synonyms:
CAS NO:881192-18-3
Molecular Formula: C20H20N2O3
Molecular Weight: 336.39
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(1H)-Pyridinone, 3-acetyl-6-(1-methylethyl)-5-(3-methyl-5-isoxazolyl)-4-phenyl-(CAS DataBase Reference)
NIST Chemistry Reference: 2(1H)-Pyridinone, 3-acetyl-6-(1-methylethyl)-5-(3-methyl-5-isoxazolyl)-4-phenyl-(881192-18-3)
EPA Substance Registry System: 2(1H)-Pyridinone, 3-acetyl-6-(1-methylethyl)-5-(3-methyl-5-isoxazolyl)-4-phenyl-(881192-18-3)

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: 881192-18-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 881192-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,1,9 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 881192-18:
(8*8)+(7*8)+(6*1)+(5*1)+(4*9)+(3*2)+(2*1)+(1*8)=183
183 % 10 = 3
So 881192-18-3 is a valid CAS Registry Number.

881192-18-3Upstream product

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881192-18-3Relevant academic research and scientific papers

Synthesis of novel 5-acetoacetyl-3-acetyl-2-pyridone derivatives by the ring-transformation of 6-methyl-1,3-oxazin-4-ones

Ouchi, Hidekazu,Saito, Hisao,Yamamoto, Yutaka,Takahata, Hiroki

, p. 299 - 308 (2007/10/03)

The synthesis of novel poly-functionalized 5-acetoacetyl-3-acetyl-2-pyridone derivatives was achieved via the ring-transformation of 6-methyl-4H-1,3-oxazin-4-ones with 3-methylisoxazole derivatives, followed by reductive cleavage of the isoxazole ring and

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