Cas 1381931-65-2,methyl 8-sec-butyl-2-oxo-6-(6-(1-p-tolylvinyl)-1,2,4-trioxan-3-yl)-2H-chromene-3-carboxylate

1381931-65-2

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Basic information

Product Name: methyl 8-sec-butyl-2-oxo-6-(6-(1-p-tolylvinyl)-1,2,4-trioxan-3-yl)-2H-chromene-3-carboxylate
Synonyms: methyl 8-sec-butyl-2-oxo-6-(6-(1-p-tolylvinyl)-1,2,4-trioxan-3-yl)-2H-chromene-3-carboxylate
CAS NO:1381931-65-2
Molecular Formula:
Molecular Weight: 464.515
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: methyl 8-sec-butyl-2-oxo-6-(6-(1-p-tolylvinyl)-1,2,4-trioxan-3-yl)-2H-chromene-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 8-sec-butyl-2-oxo-6-(6-(1-p-tolylvinyl)-1,2,4-trioxan-3-yl)-2H-chromene-3-carboxylate(1381931-65-2)
EPA Substance Registry System: methyl 8-sec-butyl-2-oxo-6-(6-(1-p-tolylvinyl)-1,2,4-trioxan-3-yl)-2H-chromene-3-carboxylate(1381931-65-2)

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: 1381931-65-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1381931-65-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,1,9,3 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1381931-65:
(9*1)+(8*3)+(7*8)+(6*1)+(5*9)+(4*3)+(3*1)+(2*6)+(1*5)=172
172 % 10 = 2
So 1381931-65-2 is a valid CAS Registry Number.

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1381931-65-2Relevant academic research and scientific papers

Coumarin-trioxane hybrids: Synthesis and evaluation as a new class of antimalarial scaffolds

Sashidhara, Koneni V.,Kumar, Abdhesh,Dodda, Ranga Prasad,Krishna, Naikade Niraj,Agarwal, Pooja,Srivastava, Kumkum,Puri

, p. 3926 - 3930 (2012/07/03)

First synthesis of novel coumarin-trioxane hybrids is reported. The synthesis was achieved via condensation of β-hydroxyhydroperoxides with coumarinic-aldehydes in presence of p-toluenesulfonic acid in good yields and the novel hybrids were evaluated for

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