Cas 1122104-64-6,(2E,2'E)-3,3'-[(5,15-diphenylporphyrinato-10,20-diyl)nickel(II)]-bis(1-(piperidin-1-yl)prop-2-en-1-one)

1122104-64-6

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Basic information

Product Name: (2E,2'E)-3,3'-[(5,15-diphenylporphyrinato-10,20-diyl)nickel(II)]-bis(1-(piperidin-1-yl)prop-2-en-1-one)
Synonyms: (2E,2'E)-3,3'-[(5,15-diphenylporphyrinato-10,20-diyl)nickel(II)]-bis(1-(piperidin-1-yl)prop-2-en-1-one)
CAS NO:1122104-64-6
Molecular Formula:
Molecular Weight: 793.59
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: (2E,2'E)-3,3'-[(5,15-diphenylporphyrinato-10,20-diyl)nickel(II)]-bis(1-(piperidin-1-yl)prop-2-en-1-one)(CAS DataBase Reference)
NIST Chemistry Reference: (2E,2'E)-3,3'-[(5,15-diphenylporphyrinato-10,20-diyl)nickel(II)]-bis(1-(piperidin-1-yl)prop-2-en-1-one)(1122104-64-6)
EPA Substance Registry System: (2E,2'E)-3,3'-[(5,15-diphenylporphyrinato-10,20-diyl)nickel(II)]-bis(1-(piperidin-1-yl)prop-2-en-1-one)(1122104-64-6)

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: 1122104-64-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1122104-64-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,2,1,0 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1122104-64:
(9*1)+(8*1)+(7*2)+(6*2)+(5*1)+(4*0)+(3*4)+(2*6)+(1*4)=76
76 % 10 = 6
So 1122104-64-6 is a valid CAS Registry Number.

1122104-64-6Upstream product

110-89-4 piperidine

1122104-64-6Downstream Products

1122104-64-6Relevant academic research and scientific papers

Synthesis, transformations, and comparative studies of porphyryl acrylic acids and their homologues

Sergeeva, Natalia N.,Bakar, Mohd B.,Senge, Mathias O.

, p. 1488 - 1497 (2009)

The reactivity of porphyryl acrylates and their homologues was studied systematically and to establish their potential as building blocks for the synthesis of novel tetrapyrroles. A new synthetic approach for multifunctional porphyrins was developed using

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