Cas 104438-89-3,2,7-Dimethyl-3-oxo-N-phenyl-2-azatricyclo<5.2.2.0<sup>1,5</sup>>undeca-4,8,10-trien-4-carboxamid

104438-89-3

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Basic information

Product Name: 2,7-Dimethyl-3-oxo-N-phenyl-2-azatricyclo<5.2.2.0^1,5>undeca-4,8,10-trien-4-carboxamid
Synonyms:
CAS NO:104438-89-3
Molecular Formula:
Molecular Weight: 306.364
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: 2,7-Dimethyl-3-oxo-N-phenyl-2-azatricyclo<5.2.2.0^1,5>undeca-4,8,10-trien-4-carboxamid(CAS DataBase Reference)
NIST Chemistry Reference: 2,7-Dimethyl-3-oxo-N-phenyl-2-azatricyclo<5.2.2.0^1,5>undeca-4,8,10-trien-4-carboxamid(104438-89-3)
EPA Substance Registry System: 2,7-Dimethyl-3-oxo-N-phenyl-2-azatricyclo<5.2.2.0^1,5>undeca-4,8,10-trien-4-carboxamid(104438-89-3)

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: 104438-89-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104438-89-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,3 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104438-89:
(8*1)+(7*0)+(6*4)+(5*4)+(4*3)+(3*8)+(2*8)+(1*9)=113
113 % 10 = 3
So 104438-89-3 is a valid CAS Registry Number.

104438-89-3Upstream product

104438-83-7 N-Methyl-N'-phenyl-N-(p-tolyl)vinylidenmalondiamid

104438-89-3Downstream Products

104438-89-3Relevant academic research and scientific papers

Cycloadditions, 11. Intramolecular Diels-Alder Reactions of Allenecarboxanilides; Synthesis and Thermolysis of Vinylidenemalondiamides

Diehl, Klaus,Himbert, Gerhard

, p. 3812 - 3825 (2007/10/02)

By known methods, phosphorus ylides are synthesized, which besides a tertiary arylcarbamoyl moiety bear an acyl group (see 2a - c), a thiocarbamoyl group (see 3), and a second, secondary carbamoyl group (see 5a - i).Only the latter compounds react with ke

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