Cas 359028-17-4,[6-diethylamino-3a,6a-dihydro-4,4-dioxo-3,6a-di(4-methoxyphenyl)-isothiazolo[5,4-d]isoxazol-3a-yl]phosphonic acid diethyl ester

359028-17-4

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Product Name: [6-diethylamino-3a,6a-dihydro-4,4-dioxo-3,6a-di(4-methoxyphenyl)-isothiazolo[5,4-d]isoxazol-3a-yl]phosphonic acid diethyl ester
Synonyms: [6-diethylamino-3a,6a-dihydro-4,4-dioxo-3,6a-di(4-methoxyphenyl)-isothiazolo[5,4-d]isoxazol-3a-yl]phosphonic acid diethyl ester
CAS NO:359028-17-4
Molecular Formula:
Molecular Weight: 579.611
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: [6-diethylamino-3a,6a-dihydro-4,4-dioxo-3,6a-di(4-methoxyphenyl)-isothiazolo[5,4-d]isoxazol-3a-yl]phosphonic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [6-diethylamino-3a,6a-dihydro-4,4-dioxo-3,6a-di(4-methoxyphenyl)-isothiazolo[5,4-d]isoxazol-3a-yl]phosphonic acid diethyl ester(359028-17-4)
EPA Substance Registry System: [6-diethylamino-3a,6a-dihydro-4,4-dioxo-3,6a-di(4-methoxyphenyl)-isothiazolo[5,4-d]isoxazol-3a-yl]phosphonic acid diethyl ester(359028-17-4)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 359028-17-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 359028-17-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,0,2 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 359028-17:
(8*3)+(7*5)+(6*9)+(5*0)+(4*2)+(3*8)+(2*1)+(1*7)=154
154 % 10 = 4
So 359028-17-4 is a valid CAS Registry Number.

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359028-17-4Relevant academic research and scientific papers

Isothiazoles. Part 12: Isothiazolylphosphonates, a new class of isothiazole dioxides

Clerici,Gelmi,Pini,Valle

, p. 5455 - 5459 (2007/10/03)

We describe a mild and efficient method to prepare 3-amino-4,5-dihydro-5-isothiazolylphosphonates from 3-amino-5-unsubstituted isothiazole dioxides. Starting from 3-amino-5-bromo-isothiazole dioxides either 3-amino-5-isothiazolylphosphonates or 5-diethoxyphosphoryl-4,5-dihydro-4-isothiazolylphosphonates were prepared. Isothiazolylphosphonates represent a new class of isothiazole dioxides. Some preliminary investigations on the reactivity with 1,3-dipoles were reported.

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