Cas 1415327-31-9,2-[(2-nitro-phenylamino)-methylene]-malonic acid monoethyl ester

1415327-31-9

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Basic information

Product Name: 2-[(2-nitro-phenylamino)-methylene]-malonic acid monoethyl ester
Synonyms: 2-[(2-nitro-phenylamino)-methylene]-malonic acid monoethyl ester
CAS NO:1415327-31-9
Molecular Formula:
Molecular Weight: 280.237
EINECS: N/A
Product Categories: N/A
Mol File: 1415327-31-9.mol
Article Data: 1

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-nitro-phenylamino)-methylene]-malonic acid monoethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(2-nitro-phenylamino)-methylene]-malonic acid monoethyl ester(1415327-31-9)
EPA Substance Registry System: 2-[(2-nitro-phenylamino)-methylene]-malonic acid monoethyl ester(1415327-31-9)

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: 1415327-31-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1415327-31-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,3,2 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1415327-31:
(9*1)+(8*4)+(7*1)+(6*5)+(5*3)+(4*2)+(3*7)+(2*3)+(1*1)=129
129 % 10 = 9
So 1415327-31-9 is a valid CAS Registry Number.

1415327-31-9Upstream product

7255-58-5 <<(2-nitropenyl)amino>methylene>propanedioic acid diethyl ester

1415327-31-9Downstream Products

1415327-31-9Relevant articles and documents

Lewis acid mediated selective monohydrolysis of geminal diesters: Synthesis of functionalized malonic acid half esters

Ilangovan, Andivelu,Kumar, Rajendranganesh,Kaushik, Mahabirprasad

supporting information, p. 2093 - 2097 (2012/11/07)

Geminal diesters, N-alkyl/aryl-2,2-bis(ethoxycarbonyl)vinylamines, were found to undergo selective hydrolysis in the presence of BF3· OEt2 at room temperature to give the corresponding half esters. Neighboring group participation by

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