Cas 506405-70-5,3-[(2-chlorophenyl)(4-hydroxy-6-methyl-2-oxo-2H-chromen-3-yl)methyl]-4-hydroxy-6-methyl-2H-chromen-2-one

506405-70-5

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Basic information

Product Name: 3-[(2-chlorophenyl)(4-hydroxy-6-methyl-2-oxo-2H-chromen-3-yl)methyl]-4-hydroxy-6-methyl-2H-chromen-2-one
Synonyms: 3-[(2-chlorophenyl)(4-hydroxy-6-methyl-2-oxo-2H-chromen-3-yl)methyl]-4-hydroxy-6-methyl-2H-chromen-2-one
CAS NO:506405-70-5
Molecular Formula: C27H19ClO6
Molecular Weight: 474.88916
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-[(2-chlorophenyl)(4-hydroxy-6-methyl-2-oxo-2H-chromen-3-yl)methyl]-4-hydroxy-6-methyl-2H-chromen-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-[(2-chlorophenyl)(4-hydroxy-6-methyl-2-oxo-2H-chromen-3-yl)methyl]-4-hydroxy-6-methyl-2H-chromen-2-one(506405-70-5)
EPA Substance Registry System: 3-[(2-chlorophenyl)(4-hydroxy-6-methyl-2-oxo-2H-chromen-3-yl)methyl]-4-hydroxy-6-methyl-2H-chromen-2-one(506405-70-5)

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: 506405-70-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 506405-70-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,6,4,0 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 506405-70:
(8*5)+(7*0)+(6*6)+(5*4)+(4*0)+(3*5)+(2*7)+(1*0)=125
125 % 10 = 5
So 506405-70-5 is a valid CAS Registry Number.

506405-70-5Upstream product

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506405-70-5Relevant academic research and scientific papers

Synthesis of monomethylated dimeric benzopyrans as HIV-1 and HIV-2 inhibitors: Part I

Chavda, Mausami,Karia, Denish,Shah, Anamik

, p. 2197 - 2199 (2007/10/03)

Mono methylated dimeric coumarins have been synthesized by condensation of 6- or 8-methyl-4-hydroxycoumarins with different aromatic aldehydes. Twenty three compounds of the two series have been screened for anti-HIV activity against HIV-1 and HIV-2 strai

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