Cas 1357787-20-2,2-methyl-N-(11-methyl-3-phenyl-6,7-dihydro-[1,3,4]oxadiazino[5,4-a]isoquinolin-1(11bH)-ylidene)propan-2-amine

1357787-20-2

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Basic information

Product Name: 2-methyl-N-(11-methyl-3-phenyl-6,7-dihydro-[1,3,4]oxadiazino[5,4-a]isoquinolin-1(11bH)-ylidene)propan-2-amine
Synonyms:
CAS NO:1357787-20-2
Molecular Formula:
Molecular Weight: 347.46
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: 2-methyl-N-(11-methyl-3-phenyl-6,7-dihydro-[1,3,4]oxadiazino[5,4-a]isoquinolin-1(11bH)-ylidene)propan-2-amine(CAS DataBase Reference)
NIST Chemistry Reference: 2-methyl-N-(11-methyl-3-phenyl-6,7-dihydro-[1,3,4]oxadiazino[5,4-a]isoquinolin-1(11bH)-ylidene)propan-2-amine(1357787-20-2)
EPA Substance Registry System: 2-methyl-N-(11-methyl-3-phenyl-6,7-dihydro-[1,3,4]oxadiazino[5,4-a]isoquinolin-1(11bH)-ylidene)propan-2-amine(1357787-20-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1357787-20-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1357787-20-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,7,8 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1357787-20:
(9*1)+(8*3)+(7*5)+(6*7)+(5*7)+(4*8)+(3*7)+(2*2)+(1*0)=202
202 % 10 = 2
So 1357787-20-2 is a valid CAS Registry Number.

1357787-20-2Upstream product

1357787-20-2Downstream Products

1357787-20-2Relevant academic research and scientific papers

[5 + 1]Cycloaddition of C,N-cyclic N′-acyl azomethine imines with isocyanides

Soeta, Takahiro,Tamura, Kaname,Ukaji, Yutaka

supporting information; experimental part, p. 1226 - 1229 (2012/05/20)

A catalyst-free [5 + 1] cycloaddition reaction between isocyanides and C,N-cyclic N′-acyl azomethine imines as the "isocyanophile" leading to novel heterocycles has been developed. These reactions proceeded quickly and cleanly to afford the corresponding

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