Cas 92919-79-4,Benzamide, N-[[2,5-dihydro-1-(4-methylphenyl)-4-[(4-methylphenyl)amino]-2,5-dioxo -1H-pyrrol-3-yl]thioxomethyl]-

92919-79-4

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Basic information

Product Name: Benzamide, N-[[2,5-dihydro-1-(4-methylphenyl)-4-[(4-methylphenyl)amino]-2,5-dioxo -1H-pyrrol-3-yl]thioxomethyl]-
Synonyms:
CAS NO:92919-79-4
Molecular Formula: C26H21N3O3S
Molecular Weight: 455.537
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: Benzamide, N-[[2,5-dihydro-1-(4-methylphenyl)-4-[(4-methylphenyl)amino]-2,5-dioxo -1H-pyrrol-3-yl]thioxomethyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Benzamide, N-[[2,5-dihydro-1-(4-methylphenyl)-4-[(4-methylphenyl)amino]-2,5-dioxo -1H-pyrrol-3-yl]thioxomethyl]-(92919-79-4)
EPA Substance Registry System: Benzamide, N-[[2,5-dihydro-1-(4-methylphenyl)-4-[(4-methylphenyl)amino]-2,5-dioxo -1H-pyrrol-3-yl]thioxomethyl]-(92919-79-4)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 92919-79-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 92919-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,1 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92919-79:
(7*9)+(6*2)+(5*9)+(4*1)+(3*9)+(2*7)+(1*9)=174
174 % 10 = 4
So 92919-79-4 is a valid CAS Registry Number.

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92919-79-4Relevant academic research and scientific papers

Electrophilic Reactions on the Maleimide Double Bond

Augustin, M.,Koehler, M.

, p. 401 - 406 (2007/10/02)

The aminosubstituted maleimides 1 are deprotonated to the anions 2, which are reacted with various electrophiles.By this way with heterocumulenes, acid chlorides and vinylogous acid chlorides the new acylated maleimides 3-6, 9, 10 are isolated.This reaction presents a method of direct acylation on the maleimide double bond.

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