Cas 607692-57-9,1H-Pyrrole-2,5-dione, 3-(methylamino)-1-(phenylmethyl)- (9CI)

607692-57-9

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Basic information

Product Name: 1H-Pyrrole-2,5-dione, 3-(methylamino)-1-(phenylmethyl)- (9CI)
Synonyms: 1H-Pyrrole-2,5-dione, 3-(methylamino)-1-(phenylmethyl)- (9CI)
CAS NO:607692-57-9
Molecular Formula: C₁₂H₁₂N₂O₂
Molecular Weight: 216.23588
EINECS: N/A
Product Categories: ALCOHOL
Mol File: 607692-57-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1H-Pyrrole-2,5-dione, 3-(methylamino)-1-(phenylmethyl)- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Pyrrole-2,5-dione, 3-(methylamino)-1-(phenylmethyl)- (9CI)(607692-57-9)
EPA Substance Registry System: 1H-Pyrrole-2,5-dione, 3-(methylamino)-1-(phenylmethyl)- (9CI)(607692-57-9)

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: 607692-57-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 607692-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,7,6,9 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 607692-57:
(8*6)+(7*0)+(6*7)+(5*6)+(4*9)+(3*2)+(2*5)+(1*7)=179
179 % 10 = 9
So 607692-57-9 is a valid CAS Registry Number.

607692-57-9Upstream product

51944-67-3 N-benzyl-3-methylpropenamide

607692-57-9Downstream Products

607692-57-9Relevant academic research and scientific papers

Formation of 3-aminofuran-2-(5 H)-ones and 3-amino-1 H -pyrrole-2,5-diones by rearrangement of isoxazolidines

Iannazzo, Daniela,Carnovale, Caterina,Giofrè, Salvatore V.,Ettari, Roberta,Romeo, Giovanni,Romeo, Roberto,Lanza, Giuseppe,Chiacchio, Ugo

, p. 245 - 248 (2011/04/22)

A novel rearrangement pathway of 3-alkoxycarbonyl-4- carbamoylisoxazolidines, leading to 1H-pyrrole-2,5-diones by treatment with TBAF, is reported. DFT quantum chemical calculations support the reaction route, controlled by ring strain, which proceeds thr

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