Cas 1056700-79-8,7-bromo-2-[6-(4-methoxy-2,6-dimethylphenyl)-pyridin-2-yl]-1,10-phenanthroline

1056700-79-8

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Basic information

Product Name: 7-bromo-2-[6-(4-methoxy-2,6-dimethylphenyl)-pyridin-2-yl]-1,10-phenanthroline
Synonyms: 7-bromo-2-[6-(4-methoxy-2,6-dimethylphenyl)-pyridin-2-yl]-1,10-phenanthroline
CAS NO:1056700-79-8
Molecular Formula:
Molecular Weight: 470.368
EINECS: N/A
Product Categories: N/A
Mol File: 1056700-79-8.mol
Article Data: 1

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: 7-bromo-2-[6-(4-methoxy-2,6-dimethylphenyl)-pyridin-2-yl]-1,10-phenanthroline(CAS DataBase Reference)
NIST Chemistry Reference: 7-bromo-2-[6-(4-methoxy-2,6-dimethylphenyl)-pyridin-2-yl]-1,10-phenanthroline(1056700-79-8)
EPA Substance Registry System: 7-bromo-2-[6-(4-methoxy-2,6-dimethylphenyl)-pyridin-2-yl]-1,10-phenanthroline(1056700-79-8)

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: 1056700-79-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1056700-79-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,6,7,0 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1056700-79:
(9*1)+(8*0)+(7*5)+(6*6)+(5*7)+(4*0)+(3*0)+(2*7)+(1*9)=138
138 % 10 = 8
So 1056700-79-8 is a valid CAS Registry Number.

1056700-79-8Upstream product

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1056700-79-8Relevant articles and documents

Synthesis of aryl-substituted 2-pyridyl-1,10-phenanthrolines; A series of oriented terpyridine analogues

Klosterman, Jeremy K.,Linden, Anthony,Siegel, Jay S.

experimental part, p. 2755 - 2764 (2009/02/02)

A 3 × 3 matrix of manisyl (4-methoxy-2,6-dimethylphenyl) substituted pyridyl-1,10-phenanthrolines has been synthesized by utilizing a general palladium catalyzed cross-coupling procedure. The directionality of these terdentate ligands will generate chiral

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