Cas 1242030-40-5,methyl 2-(anilinocarbonyl)-3-methyl-2,4a,5,6,7,8-hexahydrocinnoline-4-carboxylate

1242030-40-5

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Basic information

Product Name: methyl 2-(anilinocarbonyl)-3-methyl-2,4a,5,6,7,8-hexahydrocinnoline-4-carboxylate
Synonyms: methyl 2-(anilinocarbonyl)-3-methyl-2,4a,5,6,7,8-hexahydrocinnoline-4-carboxylate
CAS NO:1242030-40-5
Molecular Formula:
Molecular Weight: 327.383
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: methyl 2-(anilinocarbonyl)-3-methyl-2,4a,5,6,7,8-hexahydrocinnoline-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-(anilinocarbonyl)-3-methyl-2,4a,5,6,7,8-hexahydrocinnoline-4-carboxylate(1242030-40-5)
EPA Substance Registry System: methyl 2-(anilinocarbonyl)-3-methyl-2,4a,5,6,7,8-hexahydrocinnoline-4-carboxylate(1242030-40-5)

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: 1242030-40-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1242030-40-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,0,3 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1242030-40:
(9*1)+(8*2)+(7*4)+(6*2)+(5*0)+(4*3)+(3*0)+(2*4)+(1*0)=85
85 % 10 = 5
So 1242030-40-5 is a valid CAS Registry Number.

1242030-40-5Upstream product

1242030-33-6 methyl 2-(anilinocarbonyl)-3-hydroxy-3-methyl-2,3,4,4a,5,6,7,8-octahydrocinnoline-4-carboxylate

1242030-40-5Downstream Products

1242030-40-5Relevant academic research and scientific papers

Divergent base-induced reactivity of cycloalkenyl-1-diazenes

Attanasi, Orazio A.,Berretta, Stefano,De Crescentini, Lucia,Favi, Gianfranco,Filippone, Paolino,Giorgi, Gianluca,Mantellini, Fabio

experimental part, p. 6832 - 6841 (2010/09/18)

The different base-promoted regioselectivities of the ring closure processes in the reactions between cycloalkenyl-1-diazenes and β-ketoesters are investigated. Under the appropriate conditions it is possible to turn the synthesis towards cycloalkenyliden

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