Cas 936080-17-0,5-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]-3-(4-methoxyphen-yl)-4,5-dihydroisoxazole

936080-17-0

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Basic information

Product Name: 5-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]-3-(4-methoxyphen-yl)-4,5-dihydroisoxazole
Synonyms: 5-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]-3-(4-methoxyphen-yl)-4,5-dihydroisoxazole
CAS NO:936080-17-0
Molecular Formula:
Molecular Weight: 341.364
EINECS: N/A
Product Categories: N/A
Mol File: 936080-17-0.mol
Article Data: 2

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: 5-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]-3-(4-methoxyphen-yl)-4,5-dihydroisoxazole(CAS DataBase Reference)
NIST Chemistry Reference: 5-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]-3-(4-methoxyphen-yl)-4,5-dihydroisoxazole(936080-17-0)
EPA Substance Registry System: 5-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]-3-(4-methoxyphen-yl)-4,5-dihydroisoxazole(936080-17-0)

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: 936080-17-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 936080-17-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,0,8 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 936080-17:
(8*9)+(7*3)+(6*6)+(5*0)+(4*8)+(3*0)+(2*1)+(1*7)=170
170 % 10 = 0
So 936080-17-0 is a valid CAS Registry Number.

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936080-17-0Relevant articles and documents

Facile Synthesis of Natural Alkoxynaphthalene Analogues from Plant Alkoxybenzenes

Tsyganov, Dmitry V.,Krayushkin, Mikhail M.,Konyushkin, Leonid D.,Strelenko, Yuri A.,Semenova, Marina N.,Semenov, Victor V.

, p. 923 - 928 (2016/05/24)

Analogues of the bioactive natural alkoxynaphthalene pycnanthulignene D were synthesized by an efficient method. The starting plant allylalkoxybenzenes (1) are easily available from the plant essential oils of sassafras, dill, and parsley. The target 1-arylalkoxynaphthalenes (5) exhibited antiproliferative activity in a phenotypic sea urchin embryo assay.

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