Cas 1145658-92-9,4',6'-bis-(p-(dodecyloxy)phenylethynyl)-4,4''-dimethoxy-[1,1':3',1'']terphenyl

1145658-92-9

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Basic information

Product Name: 4',6'-bis-(p-(dodecyloxy)phenylethynyl)-4,4''-dimethoxy-[1,1':3',1'']terphenyl
Synonyms: 4',6'-bis-(p-(dodecyloxy)phenylethynyl)-4,4''-dimethoxy-[1,1':3',1'']terphenyl
CAS NO:1145658-92-9
Molecular Formula:
Molecular Weight: 859.245
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: 4',6'-bis-(p-(dodecyloxy)phenylethynyl)-4,4''-dimethoxy-[1,1':3',1'']terphenyl(CAS DataBase Reference)
NIST Chemistry Reference: 4',6'-bis-(p-(dodecyloxy)phenylethynyl)-4,4''-dimethoxy-[1,1':3',1'']terphenyl(1145658-92-9)
EPA Substance Registry System: 4',6'-bis-(p-(dodecyloxy)phenylethynyl)-4,4''-dimethoxy-[1,1':3',1'']terphenyl(1145658-92-9)

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: 1145658-92-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1145658-92-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,5,6,5 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1145658-92:
(9*1)+(8*1)+(7*4)+(6*5)+(5*6)+(4*5)+(3*8)+(2*9)+(1*2)=169
169 % 10 = 9
So 1145658-92-9 is a valid CAS Registry Number.

1145658-92-9Upstream product

1145658-92-9Downstream Products

1145658-93-0 C₅₈H₆₈I₂O₄

1145658-92-9Relevant academic research and scientific papers

Synthesis of j-aggregating dibenz[a,j]anthracene-based macrocycles

Chan, Julian M. W.,Tischler, Jonathan R.,Kooi, Steve E.,Bulovic, Vladimir,Swager, Timothy M.

supporting information; experimental part, p. 5659 - 5666 (2009/09/24)

Several fluorescent macrocycles based on 1,3-butadiyne-bridged dibenz[a,j]anthracene subunits have been synthesized via a multistep route. The synthetic strategy involved the initial construction of a functionalized dibenz[a,j]anthracene building block, s

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