Cas 959425-55-9,3-(2,5-diethoxyphenylthio)-5,6-dihydro-4-hydroxy-6-((naphthalen-1-yloxy)methyl)-6-phenylpyran-2-one

959425-55-9

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Basic information

Product Name: 3-(2,5-diethoxyphenylthio)-5,6-dihydro-4-hydroxy-6-((naphthalen-1-yloxy)methyl)-6-phenylpyran-2-one
Synonyms:
CAS NO:959425-55-9
Molecular Formula:
Molecular Weight: 542.653
EINECS: N/A
Product Categories: N/A
Mol File: 959425-55-9.mol
Article Data: 1

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: 3-(2,5-diethoxyphenylthio)-5,6-dihydro-4-hydroxy-6-((naphthalen-1-yloxy)methyl)-6-phenylpyran-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-(2,5-diethoxyphenylthio)-5,6-dihydro-4-hydroxy-6-((naphthalen-1-yloxy)methyl)-6-phenylpyran-2-one(959425-55-9)
EPA Substance Registry System: 3-(2,5-diethoxyphenylthio)-5,6-dihydro-4-hydroxy-6-((naphthalen-1-yloxy)methyl)-6-phenylpyran-2-one(959425-55-9)

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: 959425-55-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 959425-55-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,4,2 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 959425-55:
(8*9)+(7*5)+(6*9)+(5*4)+(4*2)+(3*5)+(2*5)+(1*5)=219
219 % 10 = 9
So 959425-55-9 is a valid CAS Registry Number.

959425-55-9Upstream product

959425-55-9Downstream Products

959425-55-9Relevant articles and documents

Modification and biological evaluation of novel 4-hydroxy-pyrone derivatives as non-peptidic HIV-1 protease inhibitors

He, Meizi,Yang, Ning,Sun, Chunlai,Yao, Xiaojian,Yang, Ming

experimental part, p. 200 - 209 (2012/03/10)

In this study, we have modified 4-hydroxy-pyran-2-ones, especially introduced heteroatoms (S or O) into the substituents, and detected their interactions with the binding pockets of HIV-1 protease (PR). The results indicated that the ethoxyl groups at C-2

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