Cas 1449029-99-5,2-chloro-N-[(cyclohexylcarbamoyl)(4-oxo-6-phenyl-4H-pyran-2-yl)methyl]-N-phenylbenzamide

1449029-99-5

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Basic information

Product Name: 2-chloro-N-[(cyclohexylcarbamoyl)(4-oxo-6-phenyl-4H-pyran-2-yl)methyl]-N-phenylbenzamide
Synonyms: 2-chloro-N-[(cyclohexylcarbamoyl)(4-oxo-6-phenyl-4H-pyran-2-yl)methyl]-N-phenylbenzamide
CAS NO:1449029-99-5
Molecular Formula:
Molecular Weight: 541.046
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-chloro-N-[(cyclohexylcarbamoyl)(4-oxo-6-phenyl-4H-pyran-2-yl)methyl]-N-phenylbenzamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-chloro-N-[(cyclohexylcarbamoyl)(4-oxo-6-phenyl-4H-pyran-2-yl)methyl]-N-phenylbenzamide(1449029-99-5)
EPA Substance Registry System: 2-chloro-N-[(cyclohexylcarbamoyl)(4-oxo-6-phenyl-4H-pyran-2-yl)methyl]-N-phenylbenzamide(1449029-99-5)

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: 1449029-99-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1449029-99-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,0,2 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1449029-99:
(9*1)+(8*4)+(7*4)+(6*9)+(5*0)+(4*2)+(3*9)+(2*9)+(1*9)=185
185 % 10 = 5
So 1449029-99-5 is a valid CAS Registry Number.

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1449029-99-5Relevant academic research and scientific papers

Cytotoxic activity assessment, QSAR and docking study of novel bis-carboxamide derivatives of 4-pyrones synthesized by Ugi four-component reaction

Shahrisa, Aziz,Esmati, Somayeh,Miri, Ramin,Firuzi, Omidreza,Edraki, Najmeh,Nejati, Maryam

, p. 388 - 399 (2013/10/01)

Fourteen novel bis-carboxamide derivatives of 4-pyrones were designed and synthesized via Ugi four-component reactions of 4-pyrone carbaldehydes, aromatic amines, isocyanides and carboxylic acids. The cytotoxic activity of synthesized derivatives was eval

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