Cas 1256730-33-2,(bis[N-(6-pyvalamido-2-pyridylmethyl)][O-carboxamido]benzylamine)(chloro)nickelate(II)

1256730-33-2

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Basic information

Product Name: (bis[N-(6-pyvalamido-2-pyridylmethyl)][O-carboxamido]benzylamine)(chloro)nickelate(II)
Synonyms: (bis[N-(6-pyvalamido-2-pyridylmethyl)][O-carboxamido]benzylamine)(chloro)nickelate(II)
CAS NO:1256730-33-2
Molecular Formula:
Molecular Weight: 580.78
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: (bis[N-(6-pyvalamido-2-pyridylmethyl)][O-carboxamido]benzylamine)(chloro)nickelate(II)(CAS DataBase Reference)
NIST Chemistry Reference: (bis[N-(6-pyvalamido-2-pyridylmethyl)][O-carboxamido]benzylamine)(chloro)nickelate(II)(1256730-33-2)
EPA Substance Registry System: (bis[N-(6-pyvalamido-2-pyridylmethyl)][O-carboxamido]benzylamine)(chloro)nickelate(II)(1256730-33-2)

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: 1256730-33-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1256730-33-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,7,3 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1256730-33:
(9*1)+(8*2)+(7*5)+(6*6)+(5*7)+(4*3)+(3*0)+(2*3)+(1*3)=152
152 % 10 = 2
So 1256730-33-2 is a valid CAS Registry Number.

1256730-33-2Upstream product

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1256730-33-2Relevant academic research and scientific papers

Nickel(II) complexes stabilized by bis[N-(6-pivalamido-2-pyridylmethyl)] benzylamine: Synthesis and characterization of complexes stabilized by a hydrogen bonding network

Powell-Jia, Darla A.,Pham, Melinda T.-N.,Ziller, Joseph W.,Borovik

, p. 2728 - 2733 (2010)

Intramolecular hydrogen bonds in metalloproteins are key in directing reactivity yet these effects have been difficult to achieved in synthetic systems. We have been developing a synthetic system that uses hydrogen-bonding interactions to modulate the sec

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