Cas 89537-99-5,(Z)-4-[1-(2-Methoxycarbonyl-phenylamino)-meth-(Z)-ylidene]-pent-2-enedioic acid 5-methyl ester

89537-99-5

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Basic information

Product Name: (Z)-4-[1-(2-Methoxycarbonyl-phenylamino)-meth-(Z)-ylidene]-pent-2-enedioic acid 5-methyl ester
Synonyms: (Z)-4-[1-(2-Methoxycarbonyl-phenylamino)-meth-(Z)-ylidene]-pent-2-enedioic acid 5-methyl ester
CAS NO:89537-99-5
Molecular Formula:
Molecular Weight: 305.287
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: (Z)-4-[1-(2-Methoxycarbonyl-phenylamino)-meth-(Z)-ylidene]-pent-2-enedioic acid 5-methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-4-[1-(2-Methoxycarbonyl-phenylamino)-meth-(Z)-ylidene]-pent-2-enedioic acid 5-methyl ester(89537-99-5)
EPA Substance Registry System: (Z)-4-[1-(2-Methoxycarbonyl-phenylamino)-meth-(Z)-ylidene]-pent-2-enedioic acid 5-methyl ester(89537-99-5)

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: 89537-99-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89537-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,3 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89537-99:
(7*8)+(6*9)+(5*5)+(4*3)+(3*7)+(2*9)+(1*9)=195
195 % 10 = 5
So 89537-99-5 is a valid CAS Registry Number.

89537-99-5Upstream product

89537-99-5Downstream Products

89537-99-5Relevant academic research and scientific papers

279. Chemie der Cumalinsaeurederivate. I. Synthese und Diels-Alder-Reactionen von 1-Arylamino-2-methoxycarbonylbutadienen

Kvita, Vratislav,Sauter, Hanspeter,Rihs, Grete

, p. 2769 - 2777 (1983)

The nucleophilic attack of substituted anilines at position 6 of methyl coumalate (1) opens the α-pyrone ring to form 4-arylamino-3-(methoxycarbonyl)butadien-1-carboxylic acid 2 (Scheme 1).The latter are easily decarboxylated at room temperature in polar

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