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506-85-4

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506-85-4 Usage

Safety Profile

An unstable explosive sensitive to heat, shock, or friction. When heated to decomposition it emits toxic fumes of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 506-85-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 506-85:
(5*5)+(4*0)+(3*6)+(2*8)+(1*5)=64
64 % 10 = 4
So 506-85-4 is a valid CAS Registry Number.
InChI:InChI=1/CHNO/c1-2-3/h3H

506-85-4Relevant academic research and scientific papers

Pyrolysis nozzles coupled to a microwave spectrometer with stark modulation for the detection of transients species in a supersonic expansion

McNaughton, Don,Evans, Corey J.

, p. 1313 - 1327 (2007/10/03)

Two types of pyrolysis nozzles have been constructed and coupled to a new Stark modulated microwave spectrometer. The nozzles were tested on their ability to generate rotationally cooled transient species through a supersonic expansion. The transients species vinylamine, thioketene and ketene were generated and detected using nozzle temperatures ranging from 400-800°C. Pyrolysis temperatures were generally lower than those used in normal flow pyrolysis experiments and rotational temperatures of ca. 10 K were achieved. A preliminary investigation of the jet nozzle pyrolysis of 3-methyl-4-hydroxyiminoisoxaline-5-one was carried out and showed a different distribution of CHNO pyrolysis products to that observed in previous low pressure studies. by Oldenbourg Wissenschaftsverlag, Muenchen.

Reactive Nitrogenous Molecules from Meldrum's Acid Derivatives, Pyrrole-2,3-diones, and Isoxazolones

Briehl, Horst,Lukosch, Adelheid,Wentrup, Curt

, p. 2772 - 2779 (2007/10/02)

Flash vacuum pyrolysis of 5-(aminomethylidene)-2,2-dimethyl-1,3-dioxane-4,6-diones (Meldrum's acid derivatives) 12 gives 4-hydroxyquinolines/4-quinolones 15 or 3-enaminoacroleins 22 in good to excellent yields.Intermediate (aminomethylene)ketenes and imidoylketenes are directly observed and their transformation into product 22 monitored by low-temperature IR spectroscopy.Imidoylketenes are also formed and observed upon thermal CO extrusion from pyrrole-2,3-diones 16.Isocyanoamines and fulminates are generated by pyrolysis of hydrazono- or oximino-Meldrum's acid derivatives 32 and 39, monitored by IR spectroscopy, and found to rearrange to cyanamides and cyanates, depending on substituents.The thermal reactions of isoxazol-5(4H)-ones and Meldrum's acid derivatives are compared and discussed.

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