Cas 1353565-36-2,5-cyclohexyl-3-(tetrahydro-2H-pyran-2-yl)pyrrolo[1',2':1,6]pyrazino[2,3-d]pyridazine-4,6(3H,5H)-dione

1353565-36-2

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Basic information

Product Name: 5-cyclohexyl-3-(tetrahydro-2H-pyran-2-yl)pyrrolo[1',2':1,6]pyrazino[2,3-d]pyridazine-4,6(3H,5H)-dione
Synonyms: 5-cyclohexyl-3-(tetrahydro-2H-pyran-2-yl)pyrrolo[1',2':1,6]pyrazino[2,3-d]pyridazine-4,6(3H,5H)-dione
CAS NO:1353565-36-2
Molecular Formula:
Molecular Weight: 368.436
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: 5-cyclohexyl-3-(tetrahydro-2H-pyran-2-yl)pyrrolo[1',2':1,6]pyrazino[2,3-d]pyridazine-4,6(3H,5H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 5-cyclohexyl-3-(tetrahydro-2H-pyran-2-yl)pyrrolo[1',2':1,6]pyrazino[2,3-d]pyridazine-4,6(3H,5H)-dione(1353565-36-2)
EPA Substance Registry System: 5-cyclohexyl-3-(tetrahydro-2H-pyran-2-yl)pyrrolo[1',2':1,6]pyrazino[2,3-d]pyridazine-4,6(3H,5H)-dione(1353565-36-2)

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: 1353565-36-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1353565-36-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,5,6 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1353565-36:
(9*1)+(8*3)+(7*5)+(6*3)+(5*5)+(4*6)+(3*5)+(2*3)+(1*6)=162
162 % 10 = 2
So 1353565-36-2 is a valid CAS Registry Number.

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1353565-36-2Relevant academic research and scientific papers

A transition metal-free tandem process to pyrrolopyrazino[2,3-d]pyridazine- diones

Huang, Aiping,Qiao, Zhi,Zhang, Xinhai,Yu, Wei,Zheng, Qingqing,Ma, Ying,Ma, Chen

, p. 906 - 912 (2012)

A transition metal-free tandem process for the synthesis of pyrrolopyrazino[2,3-d]pyridazine-diones is described. The process is an efficient construction of this tricyclic system by a one-pot coupling/Smiles rearrangement/cyclization approach. This methodology has potential applications in the synthesis of biologically and medicinally relevant compounds.

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