Cas 1265626-80-9,N-(1-((diisopropylphosphino)oxy)-3-phenylpropan-2-yl)-2,4-dimethyl-5-phenylimidazo[1,5-b]pyridazin-7-amine

1265626-80-9

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Basic information

Product Name: N-(1-((diisopropylphosphino)oxy)-3-phenylpropan-2-yl)-2,4-dimethyl-5-phenylimidazo[1,5-b]pyridazin-7-amine
Synonyms: N-(1-((diisopropylphosphino)oxy)-3-phenylpropan-2-yl)-2,4-dimethyl-5-phenylimidazo[1,5-b]pyridazin-7-amine
CAS NO:1265626-80-9
Molecular Formula:
Molecular Weight: 488.613
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: N-(1-((diisopropylphosphino)oxy)-3-phenylpropan-2-yl)-2,4-dimethyl-5-phenylimidazo[1,5-b]pyridazin-7-amine(CAS DataBase Reference)
NIST Chemistry Reference: N-(1-((diisopropylphosphino)oxy)-3-phenylpropan-2-yl)-2,4-dimethyl-5-phenylimidazo[1,5-b]pyridazin-7-amine(1265626-80-9)
EPA Substance Registry System: N-(1-((diisopropylphosphino)oxy)-3-phenylpropan-2-yl)-2,4-dimethyl-5-phenylimidazo[1,5-b]pyridazin-7-amine(1265626-80-9)

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: 1265626-80-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1265626-80-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,5,6,2 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1265626-80:
(9*1)+(8*2)+(7*6)+(6*5)+(5*6)+(4*2)+(3*6)+(2*8)+(1*0)=169
169 % 10 = 9
So 1265626-80-9 is a valid CAS Registry Number.

1265626-80-9Upstream product

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1265626-80-9Relevant academic research and scientific papers

Novel amido-complexes for the efficient asymmetric hydrogenation of imines

Kutlescha, Kathrin,Irrgang, Torsten,Kempe, Rhett

, p. 3126 - 3130 (2010)

Novel N,N,P ligand stabilized rhodium complexes exhibiting high activities and enantioselectivities in the asymmetric hydrogenation of N-aryl imines are introduced. The ligands were synthesized from inexpensive starting materials and their modular design

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