Cas 1241901-39-2,ethyl 8-cyano-6-(2,4-dichlorophenyl)-9-methyl-7-oxo-1-oxa-2,6-diazaspiro[4.4]nona-2,8-diene-3-carboxylate

1241901-39-2

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Basic information

Product Name: ethyl 8-cyano-6-(2,4-dichlorophenyl)-9-methyl-7-oxo-1-oxa-2,6-diazaspiro[4.4]nona-2,8-diene-3-carboxylate
Synonyms:
CAS NO:1241901-39-2
Molecular Formula:
Molecular Weight: 394.214
EINECS: N/A
Product Categories: N/A
Mol File: 1241901-39-2.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: ethyl 8-cyano-6-(2,4-dichlorophenyl)-9-methyl-7-oxo-1-oxa-2,6-diazaspiro[4.4]nona-2,8-diene-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 8-cyano-6-(2,4-dichlorophenyl)-9-methyl-7-oxo-1-oxa-2,6-diazaspiro[4.4]nona-2,8-diene-3-carboxylate(1241901-39-2)
EPA Substance Registry System: ethyl 8-cyano-6-(2,4-dichlorophenyl)-9-methyl-7-oxo-1-oxa-2,6-diazaspiro[4.4]nona-2,8-diene-3-carboxylate(1241901-39-2)

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: 1241901-39-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1241901-39-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,1,9,0 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1241901-39:
(9*1)+(8*2)+(7*4)+(6*1)+(5*9)+(4*0)+(3*1)+(2*3)+(1*9)=122
122 % 10 = 2
So 1241901-39-2 is a valid CAS Registry Number.

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1241901-39-2Relevant articles and documents

Spiroheterocycles via regioselective cycloaddition reactions of nitrile oxides with 5-methylene-1H-pyrrol-2(5H)-ones

Beattie, Nicola J.,Francis, Craig L.,Liepa, Andris J.,Savage, G. Paul

experimental part, p. 445 - 451 (2010/08/06)

Substituted 5-methylene-1H-pyrrol-2(5H)-ones underwent a 1,3-dipolar cycloaddition reaction with nitrile oxides to give the corresponding spiro heterocycles. Critical to this reaction was the development of a biphasic system for base-induced dehydrohaloge

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