Cas 473536-83-3,3-(benzyloxycarbonyl-hydrazono)-2-{2-dimethylamino-5-[1-(methoxycarbonyl-hydrazono)-ethyl]-4-oxo-4,5-dihydro-selenazol-5-yl}-butyric acid methyl ester

473536-83-3

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Basic information

Product Name: 3-(benzyloxycarbonyl-hydrazono)-2-{2-dimethylamino-5-[1-(methoxycarbonyl-hydrazono)-ethyl]-4-oxo-4,5-dihydro-selenazol-5-yl}-butyric acid methyl ester
Synonyms: 3-(benzyloxycarbonyl-hydrazono)-2-{2-dimethylamino-5-[1-(methoxycarbonyl-hydrazono)-ethyl]-4-oxo-4,5-dihydro-selenazol-5-yl}-butyric acid methyl ester
CAS NO:473536-83-3
Molecular Formula:
Molecular Weight: 567.46
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: 3-(benzyloxycarbonyl-hydrazono)-2-{2-dimethylamino-5-[1-(methoxycarbonyl-hydrazono)-ethyl]-4-oxo-4,5-dihydro-selenazol-5-yl}-butyric acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-(benzyloxycarbonyl-hydrazono)-2-{2-dimethylamino-5-[1-(methoxycarbonyl-hydrazono)-ethyl]-4-oxo-4,5-dihydro-selenazol-5-yl}-butyric acid methyl ester(473536-83-3)
EPA Substance Registry System: 3-(benzyloxycarbonyl-hydrazono)-2-{2-dimethylamino-5-[1-(methoxycarbonyl-hydrazono)-ethyl]-4-oxo-4,5-dihydro-selenazol-5-yl}-butyric acid methyl ester(473536-83-3)

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: 473536-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 473536-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,5,3 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 473536-83:
(8*4)+(7*7)+(6*3)+(5*5)+(4*3)+(3*6)+(2*8)+(1*3)=173
173 % 10 = 3
So 473536-83-3 is a valid CAS Registry Number.

473536-83-3Upstream product

473536-83-3Downstream Products

473536-83-3Relevant academic research and scientific papers

1,2-Diaza-1,3-butadienes: A new approach to the synthesis of selenoheterocycles

Attanasi, Orazio A.,Filippone, Paolino,Perrulli, Francesca R.,Santeusanio, Stefania

, p. 2323 - 2330 (2002)

1,2-Diaza-1,3-butadienes react easily with selenoureas to produce 2-selenazolin-4-one derivatives and with selenobenzamide to afford 2-selenazoline derivatives, the stereochemistries of which were determined. Whereas 2-selenazoline derivatives of 4R*,5R* configuration undergo aromatization under basic conditions, 2-selenazolin-4-ones, under different reaction conditions, appear to be attractive entry compounds to conjugated azoalkenes, 5,5-disubstituted selenazolin-4-ones, and spiro-condensed heterocyclic systems including selenazolinone rings. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

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