Cas 1609563-29-2,4,6,16,18-tetra(p-trifluoromethylphenylethynyl)-11,23-dimethyl-2,8,14,20-tetraoxacalix[4]arene

1609563-29-2

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Basic information

Product Name: 4,6,16,18-tetra(p-trifluoromethylphenylethynyl)-11,23-dimethyl-2,8,14,20-tetraoxacalix[4]arene
Synonyms: 4,6,16,18-tetra(p-trifluoromethylphenylethynyl)-11,23-dimethyl-2,8,14,20-tetraoxacalix[4]arene
CAS NO:1609563-29-2
Molecular Formula:
Molecular Weight: 1068.91
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: 4,6,16,18-tetra(p-trifluoromethylphenylethynyl)-11,23-dimethyl-2,8,14,20-tetraoxacalix[4]arene(CAS DataBase Reference)
NIST Chemistry Reference: 4,6,16,18-tetra(p-trifluoromethylphenylethynyl)-11,23-dimethyl-2,8,14,20-tetraoxacalix[4]arene(1609563-29-2)
EPA Substance Registry System: 4,6,16,18-tetra(p-trifluoromethylphenylethynyl)-11,23-dimethyl-2,8,14,20-tetraoxacalix[4]arene(1609563-29-2)

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: 1609563-29-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609563-29-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,5,6 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1609563-29:
(9*1)+(8*6)+(7*0)+(6*9)+(5*5)+(4*6)+(3*3)+(2*2)+(1*9)=182
182 % 10 = 2
So 1609563-29-2 is a valid CAS Registry Number.

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1609563-29-2Relevant academic research and scientific papers

Single step synthesis of acetylene-substituted oxacalix[4]arenes

Wackerly, Jay Wm.,Zhang, Mengfei,Nodder, Stephen T.,Carlin, Stephen M.,Katz, Jeffrey L.

supporting information, p. 2920 - 2922 (2014/06/23)

Oxacalixarenes bearing acetylene groups are synthesized in a single step by nucleophilic aromatic substitution reactions of orcinol with various 1,5-diethynyl-2,4-difluorobenzenes. Thermodynamic equilibration of the cyclooligomer mixtures was accomplished

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