Cas 124720-34-9,{2-(2,2-diphenylacetyl)-4-methyl-6,6-diphenyl-2-azatricyclo{5.2.2.0(1,5)}undeca-4,8,10-trien-3-one}tricarbonyliron

124720-34-9

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Basic information

Product Name: {2-(2,2-diphenylacetyl)-4-methyl-6,6-diphenyl-2-azatricyclo{5.2.2.0(1,5)}undeca-4,8,10-trien-3-one}tricarbonyliron
Synonyms:
CAS NO:124720-34-9
Molecular Formula:
Molecular Weight: 659.521
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-(2,2-diphenylacetyl)-4-methyl-6,6-diphenyl-2-azatricyclo{5.2.2.0(1,5)}undeca-4,8,10-trien-3-one}tricarbonyliron(CAS DataBase Reference)
NIST Chemistry Reference: {2-(2,2-diphenylacetyl)-4-methyl-6,6-diphenyl-2-azatricyclo{5.2.2.0(1,5)}undeca-4,8,10-trien-3-one}tricarbonyliron(124720-34-9)
EPA Substance Registry System: {2-(2,2-diphenylacetyl)-4-methyl-6,6-diphenyl-2-azatricyclo{5.2.2.0(1,5)}undeca-4,8,10-trien-3-one}tricarbonyliron(124720-34-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 124720-34-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124720-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,7,2 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 124720-34:
(8*1)+(7*2)+(6*4)+(5*7)+(4*2)+(3*0)+(2*3)+(1*4)=99
99 % 10 = 9
So 124720-34-9 is a valid CAS Registry Number.

124720-34-9Upstream product

124720-34-9Downstream Products

124720-34-9Relevant academic research and scientific papers

72. Thermal and Photochemical Reactions of 1,2-Annelated Barrelenes and Hydrobarrelenes in the Presence of Transition-Metal Carbonyls

Trifonov, Latchezar S.,Orahovats, Alexander S.

, p. 648 - 652 (1989)

The -mediated retro-Diels-Alder reaction of the annelated barrelenes 1 afforded the 1H-indol-2(3H)-one derivatives 3 (Scheme 1), while the hydrobarrelene 4a, under the same conditions, was converted to the anilide 6 (Scheme 2); 4b remained unaff

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